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Intellectual disability
The term intellectual disability or intellectual developmental disorder is used to describe significantly sub-average intellectual and adaptive functioning based on clinical assessment and as measured by individually administered, appropriately normed, standardized and validated tests of intellectual functioning and adaptive behavior, with onset during the developmental period from infancy through adolescence.
Kokkuvõte
- Teised nimetused
- Low intelligence, Mental deficiency, Poor school performance, Nonprogressive intellectual disability
- Kehasüsteem
- Abnormality of the nervous system
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Selle lehe andmed
Lehe aadressile saab lisada .json või päringusse application/json, et lugeda seda JSON-vormingus.
library(jsonlite)
url <- "https://dantelabs.com/traits/intellectual-disability.json"
page <- fromJSON(url)
page$trait$nameIntellectual disabilityHP:0001249
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Lugege välja geenid, mis on seotud Intellectual disability-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test431 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Intellectual DisabilityReads 189 of these genesACSL4ADNPAFF2AHDC1ALKBH8ANK3About this report →
- Epilepsy (Full Panel)Reads 141 of these genesACTL6BARXATP6AP2ATP6V0A1ATP6V1AATP6V1B2About this report →
- Inherited Neurodegenerative DisordersReads 148 of these genesABHD16AAHI1ALDH18A1ALDH3A2ATN1ATP8A2About this report →
- Joubert Syndrome And Related DisordersReads 37 of these genesAHI1ARL13BARMC9B9D1CC2D2ACEP104About this report →
Show 427 more reports
- Congenital Disorders of GlycosylationReads 59 of these genesATP6AP2COG5COG8DAG1FUT8GMPPBAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 38 of these genesAHI1ATP8A2CC2D2ACEP290CWF19L1GRID2About this report →
- Rare Hereditary Peripheral NeuropathiesReads 76 of these genesAIFM1FDXRHK1HPDLKIF1AMANBAAbout this report →
- DNA Repair DiseaseReads 32 of these genesERCC6GTF2H5RAD50RAD51DDB2ERCC1About this report →
- Bardet-Biedl and Alström SyndromesReads 23 of these genesBBIP1BBS2BBS7CEP290IFT74LZTFL1About this report →
- Lysosomal Storage DiseaseReads 35 of these genesCTSAFUCA1GLB1KCTD7MANBANAGLUAbout this report →
- Noonan SyndromeReads 20 of these genesBRAFKRASHRASMAP2K1MAP2K2MAPK1About this report →
- Fanconi AnemiaReads 18 of these genesRAD51ERCC4FANCBBRCA1BRCA2BRIP1About this report →
- Leber Congenital Amaurosis & RPE65-Related RetinopathyReads 19 of these genesCEP290AIPL1CRB1CRXGUCY2DIMPDH1About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 19 of these genesRBM28PTCH1ROBO1SOX3CDONDISP1About this report →
- Hereditary Spastic ParaplegiaReads 30 of these genesABHD16AALDH18A1ERLIN2GPT2HPDLKIDINS220About this report →
- Other Inherited LeukodystrophiesReads 32 of these genesALDH3A2HYCC1PEX11BPEX12PLP1POLR3BAbout this report →
- Lissencephaly Spectrum DisordersReads 17 of these genesACTG1APC2ARXLAMB1PSPHTMTC3About this report →
- Primary Mitochondrial DiseaseReads 40 of these genesAIFM1DNA2LYRM7MRPS2NDUFA2TACO1About this report →
- Congenital Muscular DystrophiesReads 18 of these genesB3GALNT2CHKBDAG1GMPPBPOMT1B4GAT1About this report →
- Coffin-Siris SyndromeReads 11 of these genesARID1ABICRADPF2SMARCA4SMARCC2SMARCD1About this report →
- GPI Anchor Biosynthesis DefectsReads 14 of these genesPIGBPIGCPIGLPIGOPIGTPIGVAbout this report →
- Hypertrophic CardiomyopathyReads 24 of these genesBRAFKRASHRASMAP2K1MAP2K2MAPK1About this report →
- Syndromic CraniosynostosisReads 14 of these genesFGFR3KAT6AFGFR1MEGF8RAB23SKIAbout this report →
- Homocystinuria & Cobalamin DisordersReads 13 of these genesCBSMMACHCMMADHCLMBRD1MTRRMAT1AAbout this report →
- Meckel SyndromeReads 9 of these genesB9D1MKS1TMEM67B9D2RPGRIP1LTCTN2About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 17 of these genesKMT2BSLC2A1WARS2ACTBKCNJ10NR4A2About this report →
- Hypogonadotropic HypogonadismReads 20 of these genesCHD7CPEMAGEL2RBM28FGFR1RAB3GAP2About this report →
- Charcot-Marie-Tooth DiseaseReads 24 of these genesAIFM1HK1MARS1NAGLUPOLR3BWARS1About this report →
- HyperinsulinismReads 9 of these genesHK1ABCC8GCKINSRKCNJ11SLC16A1About this report →
- Dyskeratosis CongenitaReads 13 of these genesZBTB24ACDDKC1PARNRTEL1TERCAbout this report →
- Retinitis PigmentosaReads 24 of these genesBBS2CC2D2AHK1ARL3OFD1POMGNT1About this report →
- Congenital HypothyroidismReads 12 of these genesTSHRFOXE1DUOX2DUOXA2IYDSECISBP2About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 14 of these genesBCORRARBERCC1ERCC2ERCC5RAB3GAP1About this report →
- Alpha-Mannosidosis and Other GlycoproteinosesReads 7 of these genesCTSAFUCA1MANBAAGAMAN2B1NAGAAbout this report →
- Urea Cycle DisorderReads 9 of these genesASLSLC25A15SLC7A7ARG1ASS1CPS1About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 12 of these genesASH1LMYT1LNFIBQRICH1RNU4-2SETD5About this report →
- Adams-Oliver SyndromeReads 6 of these genesARHGAP31DLL4DOCK6EOGTNOTCH1RBPJAbout this report →
- Cornelia de Lange SyndromeReads 6 of these genesSMC3BRD4HDAC8NIPBLRAD21SMC1AAbout this report →
- Autosomal Recessive Primary MicrocephalyReads 10 of these genesASPMCEP152CITKNL1MCPH1PDCD6IPAbout this report →
- Thyroid CancerReads 13 of these genesTSHRGNASRETDUOX2DUOXA2IYDAbout this report →
- Cutis LaxaReads 9 of these genesALDH18A1ATP6V1AATP7AELNGORABPYCR1About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 11 of these genesHYCC1PLP1POLR3BPYCR2VPS11POLR1CAbout this report →
- Leigh SyndromeReads 18 of these genesAIFM1HPDLNDUFA2PDHA1SERAC1TACO1About this report →
- Methylmalonic & Propionic AcidemiaReads 8 of these genesMMACHCMMADHCLMBRD1MMUTPCCAPCCBAbout this report →
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 8 of these genesPEX11BPEX12PEX1PEX6PEX16PEX2About this report →
- Familial Glucocorticoid DeficiencyReads 6 of these genesNDC1AAASMC2RMRAPNNTTXNRD2About this report →
- VitreoretinopathyReads 11 of these genesCOL18A1COL9A3CTNNB1DYNC1H1LRP5NDPAbout this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 8 of these genesADGRG1APC2TUBBTUBB2BTUBB3DYNC1H1About this report →
- Maturity-Onset Diabetes Of The YoungReads 7 of these genesABCC8GCKHNF4AINSKCNJ11PDX1About this report →
- Hereditary Episodic AtaxiasReads 4 of these genesCACNA1AKCNA1SCN2ASLC1A3About this report →
- Mucopolysaccharidosis Type III (Sanfilippo Syndrome)Reads 4 of these genesNAGLUHGSNATGNSSGSHAbout this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 4 of these genesDNMT3ANFIXEZH2NSD1About this report →
- Diabetes MellitusReads 11 of these genesPAX6ZBTB20ABCC8GATA6GCKHNF4AAbout this report →
- Pontocerebellar Hypoplasia (TSEN54 and MINPP1)Reads 9 of these genesAMPD2COASYPRDM13TOE1TSEN15VPS53About this report →
- Spinal Muscular AtrophyReads 10 of these genesTSEN15WARS1ATP7AASAH1DYNC1H1EMILIN1About this report →
- Classic Organic AciduriasReads 5 of these genesMLYCDIVDMCCC2ACAT1MCCC1About this report →
- Congenital Cranial Dysinnervation DisordersReads 5 of these genesTUBB3COL25A1KIF21APHOX2ATUBA1AAbout this report →
- BH4 Deficiency & Monoamine Neurotransmitter DisordersReads 6 of these genesQDPRDDCSPRPTSGCH1MAOAAbout this report →
- Alzheimer diseaseReads 4 of these genesAPPPSEN1PSEN2TREM2About this report →
- Bartter DiseaseReads 4 of these genesBSNDCLCNKBKCNJ1SLC12A1About this report →
- Periventricular Nodular HeterotopiaReads 4 of these genesFLNAMAP1BARFGEF2NEDD4LAbout this report →
- Purine & Pyrimidine Metabolism DisordersReads 5 of these genesHPRT1ADSLDPYDDPYSPRPS1About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 8 of these genesAIFM1KIF1ANTRK1TECPR2KLHL7CRLF1About this report →
- Cerebral Creatine Deficiency SyndromesReads 3 of these genesGATMSLC6A8GAMTAbout this report →
- Disorder of Copper MetabolismReads 3 of these genesAP1S1ATP7AATP7BAbout this report →
- Familial Hemiplegic MigraineReads 3 of these genesCACNA1AATP1A2SCN1AAbout this report →
- Fraser SyndromeReads 3 of these genesFRAS1FREM2GRIP1About this report →
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 3 of these genesKIFBPPHOX2BRETAbout this report →
- Megalencephalic Leukoencephalopathy with Subcortical CystsReads 3 of these genesHEPACAMGPRC5BMLC1About this report →
- Rhabdoid Tumour and SWI/SNF Tumour PredispositionReads 3 of these genesSMARCA4SMARCB1SMARCE1About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 10 of these genesATN1CACNA1ACACNA1GGRM1PUM1ITPR1About this report →
- Autism Spectrum DisorderReads 5 of these genesCHD8TBR1NLGN3NLGN4XPTCHD1About this report →
- Complex Neurodevelopmental Disorder With Motor FeaturesReads 5 of these genesCACNA1AELP2KMT2BCACNA1BEMC1About this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 5 of these genesMAGEL2NSD1H19IGF2SNRPNAbout this report →
- Neuronal Ceroid LipofuscinosisReads 6 of these genesKCTD7CLN8CLN3CLN5CTSDPPT1About this report →
- OsteopetrosisReads 6 of these genesCA2TCIRG1TNFRSF11ALRP5AMER1LRRK1About this report →
- Neonatal Diabetes MellitusReads 7 of these genesABCC8GATA6GCKINSKCNJ11PDX1About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 7 of these genesSDCCAG8TMEM67NPHP1ZNF423CEP83XPNPEP3About this report →
- Limb-Girdle Muscular DystrophyReads 9 of these genesDAG1GMPPBFKRPFKTNPOMGNT1LAMA2About this report →
- Osteogenesis ImperfectaReads 9 of these genesGORABMBTPS2PYCR1SP7ATP6V0A2LRP5About this report →
- GalactosemiaReads 3 of these genesGALEGALK1GALTAbout this report →
- NeurofibromatosisReads 3 of these genesLZTR1NF1SMARCB1About this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 3 of these genesPDE4DPRKAR1AGNASAbout this report →
- TubulinopathiesReads 3 of these genesTUBBTUBB3TUBA1AAbout this report →
- Disorders of Glycine & Serine MetabolismReads 4 of these genesPSPHSLC1A4GLDCPHGDHAbout this report →
- Carey-Fineman-Ziter SyndromeReads 2 of these genesMYMKMYMXAbout this report →
- Cowden Syndrome (PTEN hamartoma tumour syndrome)Reads 2 of these genesPTENAKT1About this report →
- DOORS SyndromeReads 2 of these genesATP6V1B2TBC1D24About this report →
- Enlarged Parietal Foramina (MSX2)Reads 2 of these genesALX4MSX2About this report →
- Fibrodysplasia Ossificans ProgressivaReads 2 of these genesGNASACVR1About this report →
- Hereditary Breast and Ovarian Cancer (BRCA1/2)Reads 2 of these genesBRCA1BRCA2About this report →
- Hereditary Multiple OsteochondromasReads 2 of these genesEXT1EXT2About this report →
- Juvenile Polyposis SyndromeReads 2 of these genesSMAD4BMPR1AAbout this report →
- Kabuki SyndromeReads 2 of these genesKDM6AKMT2DAbout this report →
- Nephrogenic Diabetes InsipidusReads 2 of these genesAQP2AVPR2About this report →
- Nevoid Basal Cell Carcinoma (Gorlin) SyndromeReads 2 of these genesPTCH1SUFUAbout this report →
- Niemann-Pick Disease Type CReads 2 of these genesNPC1NPC2About this report →
- PRR12-Related Neuroocular SyndromeReads 2 of these genesPRR12DAGLAAbout this report →
- Shwachman-Diamond SyndromeReads 2 of these genesEFL1SBDSAbout this report →
- Tuberous SclerosisReads 2 of these genesTSC1TSC2About this report →
- Wolfram Syndrome & WFS1 SpectrumReads 2 of these genesCISD2WFS1About this report →
- Inherited Congenital Heart DefectsReads 5 of these genesFLNAELNGATA6NOTCH1NKX2-5About this report →
- Inherited ThrombocytopeniasReads 8 of these genesACTBFLI1CDC42DIAPH1GALEGP1BBAbout this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 8 of these genesAP1B1MBTPS2SNAP29TATGJA1GJB3About this report →
- Congenital Myasthenic SyndromeReads 7 of these genesGMPPBALG2SLC5A7COL13A1COLQSCN4AAbout this report →
- Hereditary Methaemoglobinaemia and Unstable HaemoglobinsReads 3 of these genesHBA1HBA2CYB5R3About this report →
- Mosaic Variegated Aneuploidy SyndromeReads 3 of these genesCEP57BUB1BTRIP13About this report →
- MTOR Pathway Megalencephaly and Overgrowth DisordersReads 3 of these genesMTORPIK3CAAKT3About this report →
- Pyruvate Dehydrogenase & Pyruvate Carboxylase DeficiencyReads 4 of these genesPDHA1PCPDHXPDP1About this report →
- Parkinson DiseaseReads 5 of these genesFBXO7DNAJC6SYNJ1GBA1PLA2G6About this report →
- Dilated CardiomyopathyReads 9 of these genesFKTNPRDM16RAF1DOLKLMNAPPP1R13LAbout this report →
- Marfan Like SyndromesReads 4 of these genesFBN1SKITGFBR2TGFBR1About this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 4 of these genesCOASYDCAF17WDR45PLA2G6About this report →
- Hereditary Hypotrichosis, Woolly Hair and MonilethrixReads 5 of these genesLSSDSG4KRT81KRT83KRT86About this report →
- Growth Hormone Insensitivity & IGF-1 Axis DisordersReads 3 of these genesIGF1IGF1RGHRAbout this report →
- Rare Inherited Bone Marrow Failure SyndromesReads 3 of these genesADH5MYSM1DNAJC21About this report →
- Type I InterferonopathiesReads 4 of these genesPOLA1PSMB8ACP5IFIH1About this report →
- Urinary and Renal System TumourReads 4 of these genesTP53PAX6RETBAP1About this report →
- Hereditary Fructose Intolerance & Gluconeogenesis DefectsReads 2 of these genesFBP1ALDOBAbout this report →
- Immuno-Osseous DysplasiasReads 2 of these genesRNU4ATACRMRPAbout this report →
- MedulloblastomaReads 2 of these genesSUFUGPR161About this report →
- Monogenic Precocious PubertyReads 2 of these genesMKRN3DLK1About this report →
- Rothmund-Thomson SyndromeReads 2 of these genesRECQL4ANAPC1About this report →
- Thyroid Hormone Resistance, Transport & Metabolism DefectsReads 2 of these genesSLC16A2SECISBP2About this report →
- TyrosinemiaReads 2 of these genesTATHPDAbout this report →
- Waardenburg SyndromeReads 3 of these genesSOX10PAX3SNAI2About this report →
- Aortic AneurysmReads 4 of these genesFBN1ACTA2TGFBR2TGFBR1About this report →
- Frontotemporal DementiaReads 4 of these genesHNRNPA1HNRNPA2B1PSEN1VCPAbout this report →
- Other Inborn Errors of ImmunityReads 16 of these genesBCL11BKRASMAGT1LYSTNCF1TBX1About this report →
- Pyruvate Kinase Deficiency and Other Red Cell Enzyme DisordersReads 3 of these genesHK1GCLCGPIAbout this report →
- Glycogen Storage DiseaseReads 4 of these genesGBE1PGK1PHKA2PHKG2About this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 4 of these genesADAMTS3CCBE1FAT4KIF11About this report →
- Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome & AniridiaReads 3 of these genesITPR1PAX6PITX3About this report →
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 3 of these genesBRIP1PALB2RAD51CAbout this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 3 of these genesCOL9A3XYLT1COL2A1About this report →
- Familial Pulmonary FibrosisReads 3 of these genesPARNRTEL1TERTAbout this report →
- Kidney CancerReads 3 of these genesTP53PAX6BAP1About this report →
- Adult-Onset Leukodystrophies (CSF1R, LMNB1, Nasu-Hakola)Reads 2 of these genesCSF1RTREM2About this report →
- Complex Neurodevelopmental Disorder (TRRAP, MYH10, RERE, SOX11)Reads 2 of these genesRERETRRAPAbout this report →
- Fanconi Renotubular Syndrome and Renal GlucosuriaReads 2 of these genesGATMHNF4AAbout this report →
- Molybdenum Cofactor & Isolated Sulfite Oxidase DeficiencyReads 2 of these genesGPHNMOCS1About this report →
- Moyamoya DiseaseReads 2 of these genesACTA2RNF213About this report →
- Treacher Collins SyndromeReads 2 of these genesPOLR1CTCOF1About this report →
- 2-Aminoadipic 2-Oxoadipic AciduriaReads 1 of these genesDHTKD1About this report →
- 22q11.2 Deletion SyndromeReads 1 of these genesTBX1About this report →
- 3MC Syndrome 1 (MASP1)Reads 1 of these genesMASP1About this report →
- Acid Sphingomyelinase Deficiency (Niemann-Pick Disease Types A and B)Reads 1 of these genesSMPD1About this report →
- Acromelic Frontonasal DysostosisReads 1 of these genesZSWIM6About this report →
- ADCY5-Related DyskinesiaReads 1 of these genesADCY5About this report →
- Alacrima, Achalasia and Intellectual Disability Syndrome (GMPPA)Reads 1 of these genesGMPPAAbout this report →
- Alkuraya-Kucinskas SyndromeReads 1 of these genesBLTP1About this report →
- Angelman SyndromeReads 1 of these genesUBE3AAbout this report →
- ARC Syndrome 1 (VPS33B)Reads 1 of these genesVPS33BAbout this report →
- ARC Syndrome 2 (VIPAS39)Reads 1 of these genesVIPAS39About this report →
- ATP1A2-Related Fetal Akinesia with PolymicrogyriaReads 1 of these genesATP1A2About this report →
- Au-Kline SyndromeReads 1 of these genesHNRNPKAbout this report →
- Bailey-Bloch Congenital MyopathyReads 1 of these genesSTAC3About this report →
- BAP1 Tumour Predisposition SyndromeReads 1 of these genesBAP1About this report →
- Basilicata-Akhtar SyndromeReads 1 of these genesMSL3About this report →
- BCKDK DeficiencyReads 1 of these genesBCKDKAbout this report →
- Beaulieu-Boycott-Innes Syndrome (THOC6)Reads 1 of these genesTHOC6About this report →
- Beck-Fahrner SyndromeReads 1 of these genesTET3About this report →
- Bent Bone Dysplasia Syndrome (FGFR2)Reads 1 of these genesFGFR2About this report →
- Beta-ureidopropionase deficiencyReads 1 of these genesUPB1About this report →
- Björnstad SyndromeReads 1 of these genesBCS1LAbout this report →
- Brain Abnormalities, Neurodegeneration and Dysosteosclerosis (BANDDOS)Reads 1 of these genesCSF1RAbout this report →
- BRAT1-Related Neurodevelopmental Disorder with Cerebellar AtrophyReads 1 of these genesBRAT1About this report →
- Cardiac-Urogenital SyndromeReads 1 of these genesMYRFAbout this report →
- CDH2-Related ACOGSReads 1 of these genesCDH2About this report →
- CEBALID Syndrome (MN1)Reads 1 of these genesMN1About this report →
- CEP290-Related CiliopathyReads 1 of these genesCEP290About this report →
- Cerebrotendinous XanthomatosisReads 1 of these genesCYP27A1About this report →
- CHARGE SyndromeReads 1 of these genesCHD7About this report →
- Chediak-Higashi syndromeReads 1 of these genesLYSTAbout this report →
- Christianson SyndromeReads 1 of these genesSLC9A6About this report →
- Chung-Jansen Syndrome (PHIP)Reads 1 of these genesPHIPAbout this report →
- COL4A1-Related DisorderReads 1 of these genesCOL4A1About this report →
- Congenital Central Hypoventilation SyndromeReads 1 of these genesPHOX2BAbout this report →
- Craniofrontonasal SyndromeReads 1 of these genesEFNB1About this report →
- CTNNB1 SyndromeReads 1 of these genesCTNNB1About this report →
- Curry-Jones Syndrome (Mosaic SMO Syndrome)Reads 1 of these genesSMOAbout this report →
- CWC27-Related Retinitis Pigmentosa with Skeletal AnomaliesReads 1 of these genesCWC27About this report →
- CystathioninuriaReads 1 of these genesCTHAbout this report →
- Danon DiseaseReads 1 of these genesLAMP2About this report →
- DCC-Related Mirror Movements and Agenesis of the Corpus CallosumReads 1 of these genesDCCAbout this report →
- DeSanto-Shinawi SyndromeReads 1 of these genesWACAbout this report →
- Desbuquois Dysplasia 1Reads 1 of these genesCANT1About this report →
- DesmosterolosisReads 1 of these genesDHCR24About this report →
- DHX30-Related Neurodevelopmental DisorderReads 1 of these genesDHX30About this report →
- DIAPH1-Related Microcephaly, Seizures and Cortical BlindnessReads 1 of these genesDIAPH1About this report →
- Dias-Logan SyndromeReads 1 of these genesBCL11AAbout this report →
- DLL1-Related Neurodevelopmental DisorderReads 1 of these genesDLL1About this report →
- DPH1-Related Developmental Delay with Short StatureReads 1 of these genesDPH1About this report →
- Dravet SyndromeReads 1 of these genesSCN1AAbout this report →
- Dyssegmental Dysplasia, Silverman-Handmaker TypeReads 1 of these genesHSPG2About this report →
- EBF3-Related Neurodevelopmental Disorder (HADDS)Reads 1 of these genesEBF3About this report →
- Elsahy-Waters SyndromeReads 1 of these genesCDH11About this report →
- FANCM-Related Genomic Instability DisorderReads 1 of these genesFANCMAbout this report →
- FAT4-Related Neurodevelopmental DisorderReads 1 of these genesFAT4About this report →
- FDXR-Related Mitochondrial DisorderReads 1 of these genesFDXRAbout this report →
- Feingold Syndrome Type 1Reads 1 of these genesMYCNAbout this report →
- Ferguson-Smith Disease (Multiple Self-Healing Squamous Epithelioma)Reads 1 of these genesTGFBR1About this report →
- FGFR3-Related Chondrodysplasias (Achondroplasia and Related Conditions)Reads 1 of these genesFGFR3About this report →
- Floating-Harbor SyndromeReads 1 of these genesSRCAPAbout this report →
- Focal Dermal Hypoplasia (Goltz Syndrome)Reads 1 of these genesPORCNAbout this report →
- FOXP2-Related Speech and Language DisorderReads 1 of these genesFOXP2About this report →
- Frontonasal Dysplasia 3 (ALX1)Reads 1 of these genesALX1About this report →
- Frontonasal Dysplasia with Alopecia and Genital Anomaly (ALX4)Reads 1 of these genesALX4About this report →
- FrontorhinyReads 1 of these genesALX3About this report →
- GAPO SyndromeReads 1 of these genesANTXR1About this report →
- Gaucher DiseaseReads 1 of these genesGBA1About this report →
- Glutathione Synthetase DeficiencyReads 1 of these genesGSSAbout this report →
- Glycerol Kinase DeficiencyReads 1 of these genesGKAbout this report →
- GM1 Gangliosidosis and Morquio B SyndromeReads 1 of these genesGLB1About this report →
- Greig Cephalopolysyndactyly SyndromeReads 1 of these genesGLI3About this report →
- GRIA2-Related Neurodevelopmental DisorderReads 1 of these genesGRIA2About this report →
- GTP Cyclohydrolase 1 DeficiencyReads 1 of these genesGCH1About this report →
- GUCY2D-Related Dominant Cone-Rod DystrophyReads 1 of these genesGUCY2DAbout this report →
- GUCY2D-Related Recessive RetinopathyReads 1 of these genesGUCY2DAbout this report →
- H SyndromeReads 1 of these genesSLC29A3About this report →
- HAAO-Related Congenital NAD DeficiencyReads 1 of these genesHAAOAbout this report →
- Hao-Fountain SyndromeReads 1 of these genesUSP7About this report →
- Hartnup DiseaseReads 1 of these genesSLC6A19About this report →
- Hereditary Folate MalabsorptionReads 1 of these genesSLC46A1About this report →
- Hereditary RetinoblastomaReads 1 of these genesRB1About this report →
- HSD10 Mitochondrial DiseaseReads 1 of these genesHSD17B10About this report →
- Hyperekplexia 3 (SLC6A5)Reads 1 of these genesSLC6A5About this report →
- HyperlysinaemiaReads 1 of these genesAASSAbout this report →
- Hyperprolinaemia Type 1Reads 1 of these genesPRODHAbout this report →
- Hyperprolinaemia Type 2Reads 1 of these genesALDH4A1About this report →
- Ichthyosis VulgarisReads 1 of these genesFLGAbout this report →
- IFAP Syndrome (MBTPS2)Reads 1 of these genesMBTPS2About this report →
- IFT140-Related CiliopathyReads 1 of these genesIFT140About this report →
- JARID2-Related Neurodevelopmental DisorderReads 1 of these genesJARID2About this report →
- Johanson-Blizzard SyndromeReads 1 of these genesUBR1About this report →
- KAT6B-Related DisordersReads 1 of these genesKAT6BAbout this report →
- Kaufman Oculocerebrofacial SyndromeReads 1 of these genesUBE3BAbout this report →
- KCNH1-Related DisorderReads 1 of these genesKCNH1About this report →
- KCNQ2-Related Neonatal Encephalopathy with Non-Epileptic MyoclonusReads 1 of these genesKCNQ2About this report →
- KIDINS220-Related Ventriculomegaly and ArthrogryposisReads 1 of these genesKIDINS220About this report →
- Kohlschütter-Tönz SyndromeReads 1 of these genesROGDIAbout this report →
- KYNU-Related Congenital NAD DeficiencyReads 1 of these genesKYNUAbout this report →
- L1 SyndromeReads 1 of these genesL1CAMAbout this report →
- Lamb-Shaffer SyndromeReads 1 of these genesSOX5About this report →
- Lessel-Kreienkamp SyndromeReads 1 of these genesAGO2About this report →
- Li-Fraumeni SyndromeReads 1 of these genesTP53About this report →
- Mandibulofacial Dysostosis with MicrocephalyReads 1 of these genesEFTUD2About this report →
- Marshall-Smith SyndromeReads 1 of these genesNFIXAbout this report →
- MCM3AP-Related Peripheral NeuropathyReads 1 of these genesMCM3APAbout this report →
- MCPH1-Related Primary MicrocephalyReads 1 of these genesMCPH1About this report →
- MED27-Related Neurodevelopmental DisorderReads 1 of these genesMED27About this report →
- Meier-Gorlin Syndrome 3 (ORC6)Reads 1 of these genesORC6About this report →
- Meier-Gorlin Syndrome 4Reads 1 of these genesCDT1About this report →
- Meier-Gorlin Syndrome 7 (CDC45)Reads 1 of these genesCDC45About this report →
- MEND SyndromeReads 1 of these genesEBPAbout this report →
- Microcephalic Osteodysplastic Primordial Dwarfism Type IIReads 1 of these genesPCNTAbout this report →
- Microcephaly and Chorioretinopathy 1 (TUBGCP6)Reads 1 of these genesTUBGCP6About this report →
- Mitchell SyndromeReads 1 of these genesACOX1About this report →
- Mowat-Wilson SyndromeReads 1 of these genesZEB2About this report →
- Mucopolysaccharidosis Type I (Hurler and Scheie Syndromes)Reads 1 of these genesIDUAAbout this report →
- Mucopolysaccharidosis Type VII (Sly Syndrome)Reads 1 of these genesGUSBAbout this report →
- Nance-Horan SyndromeReads 1 of these genesNHSAbout this report →
- NDE1-Related MicrolissencephalyReads 1 of these genesNDE1About this report →
- Neurooculocardiogenitourinary Syndrome (WDR37)Reads 1 of these genesWDR37About this report →
- NFIA-Related Brain MalformationsReads 1 of these genesNFIAAbout this report →
- NGLY1 DeficiencyReads 1 of these genesNGLY1About this report →
- Nizon-Isidor SyndromeReads 1 of these genesMED12LAbout this report →
- OFD1-Related CiliopathyReads 1 of these genesOFD1About this report →
- OPA1-Related Optic AtrophyReads 1 of these genesOPA1About this report →
- Orofaciodigital Syndrome Type 14Reads 1 of these genesC2CD3About this report →
- P5CS Deficiency (ALDH18A1-Related)Reads 1 of these genesALDH18A1About this report →
- PALB2 related diseasesReads 1 of these genesPALB2About this report →
- PDX1-Related Pancreatic AgenesisReads 1 of these genesPDX1About this report →
- Pendred SyndromeReads 1 of these genesSLC26A4About this report →
- Perlman SyndromeReads 1 of these genesDIS3L2About this report →
- Phenylketonuria (PKU)Reads 1 of these genesPAHAbout this report →
- PNPLA6-Related Ataxia, Retinal Dystrophy and HypogonadismReads 1 of these genesPNPLA6About this report →
- Poirier-Bienvenu Neurodevelopmental SyndromeReads 1 of these genesCSNK2BAbout this report →
- POLR1C-Related DisorderReads 1 of these genesPOLR1CAbout this report →
- POLR3A-Related DisorderReads 1 of these genesPOLR3AAbout this report →
- POLR3B-Related DisorderReads 1 of these genesPOLR3BAbout this report →
- Pompe DiseaseReads 1 of these genesGAAAbout this report →
- Primrose SyndromeReads 1 of these genesZBTB20About this report →
- Prolidase DeficiencyReads 1 of these genesPEPDAbout this report →
- Purine Nucleoside Phosphorylase DeficiencyReads 1 of these genesPNPAbout this report →
- Radio-Tartaglia SyndromeReads 1 of these genesSPENAbout this report →
- RDH12-Related Early-Onset Retinal DystrophyReads 1 of these genesRDH12About this report →
- Rett Syndrome and MECP2-Related DisordersReads 1 of these genesMECP2About this report →
- RNU4ATAC Spectrum DisorderReads 1 of these genesRNU4ATACAbout this report →
- Roberts SyndromeReads 1 of these genesESCO2About this report →
- Salla Disease and Free Sialic Acid Storage DiseaseReads 1 of these genesSLC17A5About this report →
- Schwartz-Jampel Syndrome Type 1Reads 1 of these genesHSPG2About this report →
- SCN4A-Related Congenital MyopathyReads 1 of these genesSCN4AAbout this report →
- SF3B4-Related Acrofacial Dysostosis (Nager Syndrome)Reads 1 of these genesSF3B4About this report →
- Simpson-Golabi-Behmel SyndromeReads 1 of these genesGPC3About this report →
- Skraban-Deardorff SyndromeReads 1 of these genesWDR26About this report →
- Smith-Lemli-Opitz SyndromeReads 1 of these genesDHCR7About this report →
- Snijders Blok-Campeau SyndromeReads 1 of these genesCHD3About this report →
- Spondyloepimetaphyseal Dysplasia, Genevieve TypeReads 1 of these genesNANSAbout this report →
- Spondylometaphyseal Dysplasia With Cone-Rod DystrophyReads 1 of these genesPCYT1AAbout this report →
- SPOP-Related Neurodevelopmental Disorder with MacrocephalyReads 1 of these genesSPOPAbout this report →
- SPTBN1-Related Neurodevelopmental DisorderReads 1 of these genesSPTBN1About this report →
- Stankiewicz-Isidor SyndromeReads 1 of these genesPSMD12About this report →
- Succinic Semialdehyde Dehydrogenase DeficiencyReads 1 of these genesALDH5A1About this report →
- TANC2-Related Neurodevelopmental DisorderReads 1 of these genesTANC2About this report →
- TARP SyndromeReads 1 of these genesRBM10About this report →
- Townes-Brocks SyndromeReads 1 of these genesSALL1About this report →
- TRAPPC9-Related Intellectual DisabilityReads 1 of these genesTRAPPC9About this report →
- TRIM8-Related Neurodevelopmental and Kidney DisorderReads 1 of these genesTRIM8About this report →
- TUBB4B-Related CiliopathyReads 1 of these genesTUBB4BAbout this report →
- Turnpenny-Fry SyndromeReads 1 of these genesPCGF2About this report →
- UNC13A-Related Neurodevelopmental DisordersReads 1 of these genesUNC13AAbout this report →
- VARS1-Related Neurodevelopmental DisorderReads 1 of these genesVARS1About this report →
- Vici SyndromeReads 1 of these genesEPG5About this report →
- VPS11-Related LeukodystrophyReads 1 of these genesVPS11About this report →
- Warsaw Breakage SyndromeReads 1 of these genesDDX11About this report →
- Wiedemann-Steiner SyndromeReads 1 of these genesKMT2AAbout this report →
- Wilson DiseaseReads 1 of these genesATP7BAbout this report →
- X-linked Autoinflammatory DiseaseReads 1 of these genesIKBKGAbout this report →
- X-Linked Opitz G/BBB SyndromeReads 1 of these genesMID1About this report →
- You-Hoover-Fong Syndrome (TELO2)Reads 1 of these genesTELO2About this report →
- ZIC1-Related CraniosynostosisReads 1 of these genesZIC1About this report →
- ZTTK SyndromeReads 1 of these genesSONAbout this report →
- Female InfertilityReads 7 of these genesNUP107FANCMTRIP13TP63STARGALTAbout this report →
- Nephrotic SyndromeReads 5 of these genesNUP107NUP85PODXLLAMB2ARHGDIAAbout this report →
- Distal MyopathiesReads 4 of these genesDNAJB4HNRNPA1HNRNPA2B1VCPAbout this report →
- Hearing Loss and DeafnessReads 9 of these genesACTG1AIFM1TBC1D24DIAPH1MAP1BPRPS1About this report →
- Arrhythmogenic CardiomyopathyReads 3 of these genesCDH2PPP1R13LTMEM43About this report →
- Sclerosing Bone Dysplasias (High Bone Mass)Reads 2 of these genesSOSTLRP5About this report →
- ThalassaemiaReads 2 of these genesHBA1HBA2About this report →
- Hereditary Congenital & Juvenile CataractReads 4 of these genesLSSMAFWFS1PITX3About this report →
- Hereditary Optic NeuropathyReads 3 of these genesATP1A3OPA3OPA1About this report →
- Hereditary Periodic Fever SyndromesReads 2 of these genesMVKNLRP3About this report →
- Loeys-Dietz SyndromeReads 2 of these genesTGFBR2TGFBR1About this report →
- Peroxisomal Enzyme Disorders & Refsum DiseaseReads 2 of these genesACOX1GNPATAbout this report →
- Renal Tubular AcidosisReads 2 of these genesSLC4A4FOXI1About this report →
- Congenital Adrenal HyperplasiaReads 2 of these genesSTARPORAbout this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 2 of these genesEVCEVC2About this report →
- Hyper-IgE SyndromeReads 2 of these genesSTAT3SPINK5About this report →
- Inherited Predisposition to Acute Myeloid LeukaemiaReads 2 of these genesTERCTERTAbout this report →
- Monogenic Obesity (Leptin-Melanocortin Pathway)Reads 2 of these genesSIM1CEP19About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 4 of these genesFIG4SPG11HNRNPA1VCPAbout this report →
- Ectodermal DysplasiasReads 3 of these genesNECTIN1IKBKGTP63About this report →
- Hereditary Sideroblastic AnaemiasReads 2 of these genesPUS1YARS2About this report →
- Malignant Endocrine NeoplasmReads 2 of these genesTP53RETAbout this report →
- PolycythemiaReads 2 of these genesHBA1HBA2About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 2 of these genesCACNA1DLMNAAbout this report →
- Activated PI3K-Delta Syndrome (APDS)Reads 1 of these genesPIK3CDAbout this report →
- Biotinidase & Holocarboxylase DeficiencyReads 1 of these genesBTDAbout this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 1 of these genesNOTCH3About this report →
- CitrullinemiaReads 1 of these genesASS1About this report →
- Darier and Hailey-Hailey DiseaseReads 1 of these genesATP2A2About this report →
- Dent Disease and Lowe SyndromeReads 1 of these genesOCRLAbout this report →
- FLNB-Related Skeletal Dysplasia (Larsen Spectrum)Reads 1 of these genesFLNBAbout this report →
- Gilbert SyndromeReads 1 of these genesUGT1A1About this report →
- Hereditary FibromatosesReads 1 of these genesPDGFRBAbout this report →
- Hereditary Gingival FibromatosisReads 1 of these genesSOS1About this report →
- Hereditary Manganese Transporter DisordersReads 1 of these genesSLC39A14About this report →
- Hereditary Mixed Polyposis SyndromeReads 1 of these genesBMPR1AAbout this report →
- Hereditary Wilms TumourReads 1 of these genesWT1About this report →
- Metachromatic LeukodystrophyReads 1 of these genesARSAAbout this report →
- Müllerian Aplasia (MRKH Syndrome)Reads 1 of these genesTBX6About this report →
- Myotonic DystrophyReads 1 of these genesDMPKAbout this report →
- Neuroblastoma Predisposition (ALK and PHOX2B)Reads 1 of these genesPHOX2BAbout this report →
- Otospondylomegaepiphyseal Dysplasia (OSMED)Reads 1 of these genesCOL2A1About this report →
- Severe Inherited Insulin ResistanceReads 1 of these genesINSRAbout this report →
- STAT1 and STAT3 Gain-of-Function DiseaseReads 1 of these genesSTAT3About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 3 of these genesATRXHHATWT1About this report →
- Congenital Stationary Night BlindnessReads 3 of these genesCABP4GUCY2DPRPH2About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 4 of these genesPOLA1PSMB8ACP5IFIH1About this report →
- Hereditary Macular DystrophiesReads 2 of these genesPRDM13PRPH2About this report →
- Inherited IchthyosesReads 3 of these genesNSDHLCLDN1STSAbout this report →
- Familial HypomagnesemiaReads 2 of these genesCNNM2KCNJ10About this report →
- Polycystic Kidney DiseaseReads 2 of these genesALG9IFT140About this report →
- LipodystrophyReads 2 of these genesPLAAT3LMNAAbout this report →
- Severe Congenital NeutropeniaReads 2 of these genesHAX1CLPBAbout this report →
- Cerebral Amyloid AngiopathyReads 1 of these genesAPPAbout this report →
- Familial Periodic ParalysisReads 1 of these genesSCN4AAbout this report →
- Griscelli SyndromeReads 1 of these genesMYO5AAbout this report →
- HyperthyroidismReads 1 of these genesTSHRAbout this report →
- Leukocyte Adhesion DeficiencyReads 1 of these genesSLC35C1About this report →
- Monogenic Early-Onset OsteoporosisReads 1 of these genesCOPB2About this report →
- Mucolipidoses (ML II, ML III and ML IV)Reads 1 of these genesMCOLN1About this report →
- RDH5-Related Retinopathy (Fundus Albipunctatus)Reads 1 of these genesPRPH2About this report →
- Tetralogy of FallotReads 1 of these genesNKX2-5About this report →
- Van der Woude and Popliteal Pterygium Syndromes (IRF6)Reads 1 of these genesRIPK4About this report →
- X-Linked Lymphoproliferative Disease and XMENReads 1 of these genesMAGT1About this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 2 of these genesCACNA1DCACNA1HAbout this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 2 of these genesHADHAHADHAbout this report →
- 46,XX Differences of Sex DevelopmentReads 1 of these genesSOX3About this report →
- Achondrogenesis panelReads 1 of these genesCOL2A1About this report →
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 1 of these genesPRKAR1AAbout this report →
- Familial Atrial FibrillationReads 1 of these genesGJA5About this report →
- Familial Paget Disease of BoneReads 1 of these genesTNFRSF11AAbout this report →
- Hereditary Gastrointestinal Stromal TumourReads 1 of these genesKITAbout this report →
- Hereditary Hemorrhagic TelangiectasiaReads 1 of these genesSMAD4About this report →
- Maple Syrup Urine DiseaseReads 1 of these genesBCKDHAAbout this report →
- MelanomaReads 1 of these genesCDK4About this report →
- Multiple Synostoses Syndrome (FGF9)Reads 1 of these genesGDF6About this report →
- Polycystic Liver Disease (1 and 2)Reads 1 of these genesLRP5About this report →
- PorokeratosisReads 1 of these genesMVKAbout this report →
- Hereditary Corneal DystrophiesReads 2 of these genesMCOLN1TCF4About this report →
- Autosomal Dominant Tubulointerstitial Kidney DiseaseReads 1 of these genesHNF1BAbout this report →
- Autoimmune DiseaseReads 2 of these genesKRASSTAT3About this report →
- Ehlers-Danlos SyndromeReads 2 of these genesCOL3A1CHST14About this report →
- Chronic Granulomatous DiseaseReads 1 of these genesNCF1About this report →
- Hereditary SpherocytosisReads 1 of these genesANK1About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Surfactant Metabolism DysfunctionReads 1 of these genesMARS1About this report →
- Syndromic and Metabolic CardiomyopathiesReads 1 of these genesNKX2-5About this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesKRASAbout this report →
- Basal Ganglia CalcificationReads 1 of these genesPDGFRBAbout this report →
- Hereditary HypolipoproteinemiasReads 1 of these genesSAR1BAbout this report →
- Severe Combined ImmunodeficiencyReads 2 of these genesBCL11BLIG4About this report →
- Aicardi-Goutieres SyndromeReads 1 of these genesIFIH1About this report →
- GlomerulosclerosisReads 1 of these genesPAX2About this report →
- Hepatic Porphyria DisordersReads 1 of these genesPPOXAbout this report →
- Inherited Platelet Function DisordersReads 1 of these genesGP1BBAbout this report →
- PorphyriaReads 1 of these genesPPOXAbout this report →
- Focal Segmental GlomerulosclerosisReads 1 of these genesPAX2About this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 1 of these genesRETAbout this report →
- Long QT SyndromeReads 1 of these genesCACNA1CAbout this report →
- Male InfertilityReads 2 of these genesFKBP6FANCMAbout this report →
- Congenital Anomalies of the Kidney and Urinary TractReads 1 of these genesPAX2About this report →
- Heterotaxy & Laterality DefectsReads 1 of these genesNODALAbout this report →
- Hereditary AmyloidosisReads 1 of these genesAPPAbout this report →
- Myofibrillar MyopathiesReads 1 of these genesKYAbout this report →
- Diamond-Blackfan AnemiaReads 1 of these genesRPS19About this report →
- Amelogenesis ImperfectaReads 1 of these genesITGB6About this report →
- Epidermolysis BullosaReads 1 of these genesDSTAbout this report →
- Congenital MyopathiesReads 1 of these genesTNNT1About this report →
Lugege välja geenid, mis on seotud Intellectual disability-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test1647 geeni on seotud tunnusega Intellectual disability
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Intellectual disability. Enamikul selle tunnusega inimestest ei ole ühtegi neist haigustest. Selles loendis olev geen ei ütle midagi kellegi enda genoomi kohta.
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| ABHD16Aabhydrolase domain containing 16A, phospholipase | Alati | Esineb 1 haiguses |
| ACSL4acyl-CoA synthetase long chain family member 4 | Alati | Esineb 1 haiguses |
| ACTG1actin gamma 1 | Alati | Esineb 2 haiguses |
| ACTL6Bactin like 6B | Alati | Esineb 2 haiguses |
| ADARB1adenosine deaminase RNA specific B1 | Alati | Esineb 1 haiguses |
| ADAT3adenosine deaminase tRNA specific 3 | Alati | Esineb 2 haiguses |
| ADGRG1adhesion G protein-coupled receptor G1 | Alati | Esineb 4 haiguses |
| ADH5alcohol dehydrogenase 5 (class III), chi polypeptide | Alati | Esineb 1 haiguses |
| ADNPactivity dependent neuroprotector homeobox | Alati | Esineb 1 haiguses |
| AFF2ALF transcription elongation factor 2 | Alati | Esineb 2 haiguses |
| AFF3ALF transcription elongation factor 3 | Alati | Esineb 1 haiguses |
| AGO1argonaute RISC component 1 | Alati | Esineb 1 haiguses |
| AGO2argonaute RISC catalytic component 2 | Alati | Esineb 1 haiguses |
| AHDC1AT-hook DNA binding motif containing 1 | Alati | Esineb 2 haiguses |
| AHI1Abelson helper integration site 1 | Alati | Esineb 3 haiguses |
| AIFM1apoptosis inducing factor mitochondria associated 1 | Alati | Esineb 4 haiguses |
| ALDH18A1aldehyde dehydrogenase 18 family member A1 | Alati | Esineb 3 haiguses |
| ALDH3A2aldehyde dehydrogenase 3 family member A2 | Alati | Esineb 2 haiguses |
| ALKBH8alkB homolog 8, tRNA methyltransferase | Alati | Esineb 1 haiguses |
| ALX1ALX homeobox 1 | Alati | Esineb 2 haiguses |
| AMPD2adenosine monophosphate deaminase 2 | Alati | Esineb 1 haiguses |
| ANK3ankyrin 3 | Alati | Esineb 1 haiguses |
| ANKRD11ankyrin repeat domain 11 | Alati | Esineb 1 haiguses |
| AP1B1adaptor related protein complex 1 subunit beta 1 | Alati | Esineb 2 haiguses |
| AP1G1adaptor related protein complex 1 subunit gamma 1 | Alati | Esineb 2 haiguses |
| AP2M1adaptor related protein complex 2 subunit mu 1 | Alati | Esineb 2 haiguses |
| APC2APC regulator of Wnt signaling pathway 2 | Alati | Esineb 1 haiguses |
| AQP4aquaporin 4 | Alati | Esineb 2 haiguses |
| ARHGEF2Rho/Rac guanine nucleotide exchange factor 2 | Alati | Esineb 1 haiguses |
| ARID1AAT-rich interaction domain 1A | Alati | Esineb 1 haiguses |
| ARL13BARF like GTPase 13B | Alati | Esineb 2 haiguses |
| ARMC9armadillo repeat containing 9 | Alati | Esineb 2 haiguses |
| ARXaristaless related homeobox | Alati | Esineb 8 haiguses |
| ASH1LASH1 like histone lysine methyltransferase | Alati | Esineb 1 haiguses |
| ASPMassembly factor for spindle microtubules | Alati | Esineb 1 haiguses |
| ASXL3ASXL transcriptional regulator 3 | Alati | Esineb 2 haiguses |
| ATN1atrophin 1 | Alati | Esineb 2 haiguses |
| ATP2B1ATPase plasma membrane Ca2+ transporting 1 | Alati | Esineb 1 haiguses |
| ATP6AP2ATPase H+ transporting accessory protein 2 | Alati | Esineb 2 haiguses |
| ATP6V0A1ATPase H+ transporting V0 subunit a1 | Alati | Esineb 2 haiguses |
Näita veel 1607 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| ATP6V0CATPase H+ transporting V0 subunit c | Alati | Esineb 1 haiguses |
| ATP6V1AATPase H+ transporting V1 subunit A | Alati | Esineb 2 haiguses |
| ATP6V1B2ATPase H+ transporting V1 subunit B2 | Alati | Esineb 3 haiguses |
| ATP8A2ATPase phospholipid transporting 8A2 | Alati | Esineb 2 haiguses |
| ATRXATRX chromatin remodeler | Alati | Esineb 3 haiguses |
| B3GALNT2beta-1,3-N-acetylgalactosaminyltransferase 2 | Alati | Esineb 2 haiguses |
| B9D1B9 domain containing 1 | Alati | Esineb 2 haiguses |
| BBIP1BBSome interacting protein 1 | Alati | Esineb 2 haiguses |
| BBS2Bardet-Biedl syndrome 2 | Alati | Esineb 2 haiguses |
| BBS7Bardet-Biedl syndrome 7 | Alati | Esineb 2 haiguses |
| BCKDKbranched chain keto acid dehydrogenase kinase | Alati | Esineb 1 haiguses |
| BCL11ABCL11 transcription factor A | Alati | Esineb 1 haiguses |
| BCL11BBCL11 transcription factor B | Alati | Esineb 2 haiguses |
| BCORBCL6 corepressor | Alati | Esineb 3 haiguses |
| BICRABRD4 interacting chromatin remodeling complex associated protein | Alati | Esineb 1 haiguses |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Alati | Esineb 7 haiguses |
| BRF1BRF1 general transcription factor IIIB subunit | Alati | Esineb 1 haiguses |
| BRWD3bromodomain and WD repeat domain containing 3 | Alati | Esineb 1 haiguses |
| BUB1BUB1 mitotic checkpoint serine/threonine kinase | Alati | Esineb 2 haiguses |
| CA2carbonic anhydrase 2 | Alati | Esineb 2 haiguses |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Alati | Esineb 6 haiguses |
| CACNA1Gcalcium voltage-gated channel subunit alpha1 G | Alati | Esineb 1 haiguses |
| CAMK2Acalcium/calmodulin dependent protein kinase II alpha | Alati | Esineb 1 haiguses |
| CASP2caspase 2 | Alati | Esineb 1 haiguses |
| CBScystathionine beta-synthase | Alati | Esineb 2 haiguses |
| CC2D2Acoiled-coil and C2 domain containing 2A | Alati | Esineb 3 haiguses |
| CCT3chaperonin containing TCP1 subunit 3 | Alati | Esineb 1 haiguses |
| CDH11cadherin 11 | Alati | Esineb 2 haiguses |
| CDH15cadherin 15 | Alati | Esineb 1 haiguses |
| CDK10cyclin dependent kinase 10 | Alati | Esineb 1 haiguses |
| CDK13cyclin dependent kinase 13 | Alati | Esineb 1 haiguses |
| CDK19cyclin dependent kinase 19 | Alati | Esineb 2 haiguses |
| CDK8cyclin dependent kinase 8 | Alati | Esineb 1 haiguses |
| CELF2CUGBP Elav-like family member 2 | Alati | Esineb 2 haiguses |
| CEP104centrosomal protein 104 | Alati | Esineb 2 haiguses |
| CEP152centrosomal protein 152 | Alati | Esineb 2 haiguses |
| CEP290centrosomal protein 290 | Alati | Esineb 5 haiguses |
| CEP295centrosomal protein 295 | Alati | Esineb 2 haiguses |
| CEP57centrosomal protein 57 | Alati | Esineb 2 haiguses |
| CEP63centrosomal protein 63 | Alati | Esineb 2 haiguses |
| CERT1ceramide transporter 1 | Alati | Esineb 1 haiguses |
| CHAMP1chromosome alignment maintaining phosphoprotein 1 | Alati | Esineb 1 haiguses |
| CHD2chromodomain helicase DNA binding protein 2 | Alati | Esineb 3 haiguses |
| CHD3chromodomain helicase DNA binding protein 3 | Alati | Esineb 1 haiguses |
| CHD4chromodomain helicase DNA binding protein 4 | Alati | Esineb 1 haiguses |
| CHD7chromodomain helicase DNA binding protein 7 | Alati | Esineb 2 haiguses |
| CHD8chromodomain helicase DNA binding protein 8 | Alati | Esineb 2 haiguses |
| CHKBcholine kinase beta | Alati | Esineb 1 haiguses |
| CHP1calcineurin like EF-hand protein 1 | Alati | Esineb 1 haiguses |
| CITcitron rho-interacting serine/threonine kinase | Alati | Esineb 1 haiguses |
| CLCN3Cl-/H+ antiporter 3 | Alati | Esineb 1 haiguses |
| CLTCclathrin heavy chain | Alati | Esineb 2 haiguses |
| CNKSR2connector enhancer of kinase suppressor of Ras 2 | Alati | Esineb 2 haiguses |
| CNNM2cyclin and CBS domain divalent metal cation transport mediator 2 | Alati | Esineb 1 haiguses |
| CNTNAP2contactin associated protein 2 | Alati | Esineb 1 haiguses |
| COASYCoenzyme A synthase | Alati | Esineb 1 haiguses |
| COG3component of oligomeric golgi complex 3 | Alati | Esineb 1 haiguses |
| COG5component of oligomeric golgi complex 5 | Alati | Esineb 1 haiguses |
| COG8component of oligomeric golgi complex 8 | Alati | Esineb 2 haiguses |
| COL18A1collagen type XVIII alpha 1 chain | Alati | Esineb 1 haiguses |
| COL9A3collagen type IX alpha 3 chain | Alati | Esineb 1 haiguses |
| CPEcarboxypeptidase E | Alati | Esineb 1 haiguses |
| CPLX1complexin 1 | Alati | Esineb 2 haiguses |
| CPSF3cleavage and polyadenylation specific factor 3 | Alati | Esineb 1 haiguses |
| CRADDCARD and death domain containing adaptor protein | Alati | Esineb 1 haiguses |
| CREBBPCREB binding lysine acetyltransferase | Alati | Esineb 5 haiguses |
| CRNKL1crooked neck pre-mRNA splicing factor 1 | Alati | Esineb 1 haiguses |
| CSNK2Bcasein kinase 2 beta | Alati | Esineb 1 haiguses |
| CTCFCCCTC-binding factor | Alati | Esineb 2 haiguses |
| CTNNB1catenin beta 1 | Alati | Esineb 4 haiguses |
| CTSAcathepsin A | Alati | Esineb 2 haiguses |
| CUL4Bcullin 4B | Alati | Esineb 1 haiguses |
| CUX2cut like homeobox 2 | Alati | Esineb 2 haiguses |
| CWF19L1CWF19 like cell cycle control factor 1 | Alati | Esineb 1 haiguses |
| DAG1dystroglycan 1 | Alati | Esineb 2 haiguses |
| DDB1damage specific DNA binding protein 1 | Alati | Esineb 1 haiguses |
| DDX3XDEAD-box helicase 3 X-linked | Alati | Esineb 3 haiguses |
| DDX59DEAD-box helicase 59 | Alati | Esineb 2 haiguses |
| DDX6DEAD-box helicase 6 | Alati | Esineb 1 haiguses |
| DEAF1DEAF1 transcription factor | Alati | Esineb 3 haiguses |
| DHRS3dehydrogenase/reductase 3 | Alati | Esineb 1 haiguses |
| DHX30DExH-box helicase 30 | Alati | Esineb 1 haiguses |
| DLG3discs large MAGUK scaffold protein 3 | Alati | Esineb 1 haiguses |
| DLG4discs large MAGUK scaffold protein 4 | Alati | Esineb 1 haiguses |
| DNA2DNA replication helicase/nuclease 2 | Alati | Esineb 2 haiguses |
| DNM1dynamin 1 | Alati | Esineb 3 haiguses |
| DNMT3ADNA methyltransferase 3 alpha | Alati | Esineb 1 haiguses |
| DPF2double PHD fingers 2 | Alati | Esineb 1 haiguses |
| DPH1diphthamide biosynthesis 1 | Alati | Esineb 1 haiguses |
| DPP6dipeptidyl peptidase like 6 | Alati | Esineb 1 haiguses |
| DTYMKdeoxythymidylate kinase | Alati | Esineb 1 haiguses |
| DYMdymeclin | Alati | Esineb 2 haiguses |
| EEDembryonic ectoderm development | Alati | Esineb 1 haiguses |
| EIF4A2eukaryotic translation initiation factor 4A2 | Alati | Esineb 1 haiguses |
| ELP2elongator acetyltransferase complex subunit 2 | Alati | Esineb 1 haiguses |
| EP300EP300 lysine acetyltransferase | Alati | Esineb 4 haiguses |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Alati | Esineb 4 haiguses |
| ERI1exoribonuclease 1 | Alati | Esineb 1 haiguses |
| ERLIN2ER lipid raft associated 2 | Alati | Esineb 2 haiguses |
| EXOSC5exosome component 5 | Alati | Esineb 1 haiguses |
| FAM149B1family with sequence similarity 149 member B1 | Alati | Esineb 2 haiguses |
| FAM177A1family with sequence similarity 177 member A1 | Alati | Esineb 1 haiguses |
| FBXL3F-box and leucine rich repeat protein 3 | Alati | Esineb 1 haiguses |
| FBXO11F-box protein 11 | Alati | Esineb 1 haiguses |
| FBXO28F-box protein 28 | Alati | Esineb 2 haiguses |
| FBXO31F-box protein 31 | Alati | Esineb 1 haiguses |
| FBXO7F-box protein 7 | Alati | Esineb 1 haiguses |
| FDXRferredoxin reductase | Alati | Esineb 1 haiguses |
| FEM1Bfem-1 homolog B | Alati | Esineb 1 haiguses |
| FERRY3FERRY endosomal RAB5 effector complex subunit 3 | Alati | Esineb 1 haiguses |
| FGFR3fibroblast growth factor receptor 3 | Alati | Esineb 6 haiguses |
| FILIP1filamin A interacting protein 1 | Alati | Esineb 1 haiguses |
| FLNAfilamin A | Alati | Esineb 4 haiguses |
| FMN2formin 2 | Alati | Esineb 1 haiguses |
| FOXP1forkhead box P1 | Alati | Esineb 1 haiguses |
| FRA10AC1FRA10A associated CGG repeat 1 | Alati | Esineb 1 haiguses |
| FRMD5FERM domain containing 5 | Alati | Esineb 1 haiguses |
| FRMPD4FERM and PDZ domain containing 4 | Alati | Esineb 1 haiguses |
| FRYLFRY like transcription coactivator | Alati | Esineb 1 haiguses |
| FTSJ1FtsJ RNA 2'-O-methyltransferase 1 | Alati | Esineb 1 haiguses |
| FUCA1alpha-L-fucosidase 1 | Alati | Esineb 1 haiguses |
| FUT8fucosyltransferase 8 | Alati | Esineb 1 haiguses |
| GABBR2gamma-aminobutyric acid type B receptor subunit 2 | Alati | Esineb 4 haiguses |
| GABRA1gamma-aminobutyric acid type A receptor subunit alpha1 | Alati | Esineb 3 haiguses |
| GATMglycine amidinotransferase | Alati | Esineb 1 haiguses |
| GDI1GDP dissociation inhibitor 1 | Alati | Esineb 1 haiguses |
| GGT1gamma-glutamyltransferase 1 | Alati | Esineb 2 haiguses |
| GLB1galactosidase beta 1 | Alati | Esineb 2 haiguses |
| GMPPBGDP-mannose pyrophosphorylase B | Alati | Esineb 4 haiguses |
| GNAI1G protein subunit alpha i1 | Alati | Esineb 1 haiguses |
| GNB1G protein subunit beta 1 | Alati | Esineb 2 haiguses |
| GNB5G protein subunit beta 5 | Alati | Esineb 2 haiguses |
| GPT2glutamic--pyruvic transaminase 2 | Alati | Esineb 2 haiguses |
| GRIA1glutamate ionotropic receptor AMPA type subunit 1 | Alati | Esineb 1 haiguses |
| GRIA2glutamate ionotropic receptor AMPA type subunit 2 | Alati | Esineb 1 haiguses |
| GRIA3glutamate ionotropic receptor AMPA type subunit 3 | Alati | Esineb 1 haiguses |
| GRIA4glutamate ionotropic receptor AMPA type subunit 4 | Alati | Esineb 1 haiguses |
| GRID2glutamate ionotropic receptor delta type subunit 2 | Alati | Esineb 1 haiguses |
| GRIK2glutamate ionotropic receptor kainate type subunit 2 | Alati | Esineb 2 haiguses |
| GRIN1glutamate ionotropic receptor NMDA type subunit 1 | Alati | Esineb 2 haiguses |
| GRIN2Bglutamate ionotropic receptor NMDA type subunit 2B | Alati | Esineb 2 haiguses |
| GRM1glutamate metabotropic receptor 1 | Alati | Esineb 2 haiguses |
| GRM7glutamate metabotropic receptor 7 | Alati | Esineb 2 haiguses |
| GTF2H5general transcription factor IIH subunit 5 | Alati | Esineb 1 haiguses |
| GTF3C3general transcription factor IIIC subunit 3 | Alati | Esineb 1 haiguses |
| H1-4H1.4 linker histone, cluster member | Alati | Esineb 1 haiguses |
| H4C11H4 clustered histone 11 | Alati | Esineb 1 haiguses |
| H4C3H4 clustered histone 3 | Alati | Esineb 1 haiguses |
| H4C5H4 clustered histone 5 | Alati | Esineb 1 haiguses |
| HAX1HCLS1 associated protein X-1 | Alati | Esineb 1 haiguses |
| HCN1hyperpolarization activated cyclic nucleotide gated potassium channel 1 | Alati | Esineb 3 haiguses |
| HECTD4HECT domain E3 ubiquitin protein ligase 4 | Alati | Esineb 1 haiguses |
| HECW2HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2 | Alati | Esineb 1 haiguses |
| HERC1HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 | Alati | Esineb 1 haiguses |
| HERC2HECT and RLD domain containing E3 ubiquitin protein ligase 2 | Alati | Esineb 2 haiguses |
| HIVEP2HIVEP zinc finger 2 | Alati | Esineb 1 haiguses |
| HK1hexokinase 1 | Alati | Esineb 1 haiguses |
| HMGB3high mobility group box 3 | Alati | Esineb 1 haiguses |
| HNRNPH1heterogeneous nuclear ribonucleoprotein H1 | Alati | Esineb 1 haiguses |
| HNRNPH2heterogeneous nuclear ribonucleoprotein H2 | Alati | Esineb 1 haiguses |
| HNRNPUheterogeneous nuclear ribonucleoprotein U | Alati | Esineb 1 haiguses |
| HPDL4-hydroxyphenylpyruvate dioxygenase like | Alati | Esineb 1 haiguses |
| HPRT1hypoxanthine phosphoribosyltransferase 1 | Alati | Esineb 2 haiguses |
| HS2ST1heparan sulfate 2-O-sulfotransferase 1 | Alati | Esineb 1 haiguses |
| HSD17B10hydroxysteroid 17-beta dehydrogenase 10 | Alati | Esineb 2 haiguses |
| HUWE1HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1 | Alati | Esineb 1 haiguses |
| HYCC1hyccin PI4KA lipid kinase complex subunit 1 | Alati | Esineb 1 haiguses |
| IARS1isoleucyl-tRNA synthetase 1 | Alati | Esineb 2 haiguses |
| IFT74intraflagellar transport 74 | Alati | Esineb 4 haiguses |
| IGBP1immunoglobulin binding protein 1 | Alati | Esineb 2 haiguses |
| IGF1insulin like growth factor 1 | Alati | Esineb 2 haiguses |
| IMPA1inositol monophosphatase 1 | Alati | Esineb 1 haiguses |
| INPP4Ainositol polyphosphate-4-phosphatase type I A | Alati | Esineb 1 haiguses |
| INPP5Einositol polyphosphate-5-phosphatase E | Alati | Esineb 3 haiguses |
| IQSEC2IQ motif and Sec7 domain ArfGEF 2 | Alati | Esineb 2 haiguses |
| IRF2BPLinterferon regulatory factor 2 binding protein like | Alati | Esineb 1 haiguses |
| IRX5iroquois homeobox 5 | Alati | Esineb 1 haiguses |
| JKAMPJNK1/MAPK8 associated membrane protein | Alati | Esineb 1 haiguses |
| KAT6Alysine acetyltransferase 6A | Alati | Esineb 1 haiguses |
| KCNA4potassium voltage-gated channel subfamily A member 4 | Alati | Esineb 1 haiguses |
| KCNC2potassium voltage-gated channel subfamily C member 2 | Alati | Esineb 2 haiguses |
| KCNK4potassium two pore domain channel subfamily K member 4 | Alati | Esineb 1 haiguses |
| KCNN2potassium calcium-activated channel subfamily N member 2 | Alati | Esineb 1 haiguses |
| KCNQ2potassium voltage-gated channel subfamily Q member 2 | Alati | Esineb 2 haiguses |
| KCNQ5potassium voltage-gated channel subfamily Q member 5 | Alati | Esineb 1 haiguses |
| KCTD7potassium channel tetramerization domain containing 7 | Alati | Esineb 2 haiguses |
| KDM4Blysine demethylase 4B | Alati | Esineb 1 haiguses |
| KDM5Alysine demethylase 5A | Alati | Esineb 1 haiguses |
| KDM6Alysine demethylase 6A | Alati | Esineb 3 haiguses |
| KICS2KICSTOR subunit 2 | Alati | Esineb 1 haiguses |
| KIDINS220kinase D interacting substrate 220 | Alati | Esineb 2 haiguses |
| KIF1Akinesin family member 1A | Alati | Esineb 2 haiguses |
| KIF4Akinesin family member 4A | Alati | Esineb 1 haiguses |
| KIFBPkinesin family binding protein | Alati | Esineb 2 haiguses |
| KLHL15kelch like family member 15 | Alati | Esineb 1 haiguses |
| KMT2Alysine methyltransferase 2A | Alati | Esineb 2 haiguses |
| KMT2Blysine methyltransferase 2B | Alati | Esineb 2 haiguses |
| KMT2Clysine methyltransferase 2C | Alati | Esineb 2 haiguses |
| KMT5Blysine methyltransferase 5B | Alati | Esineb 1 haiguses |
| KNL1kinetochore scaffold 1 | Alati | Esineb 1 haiguses |
| KRASKRas proto-oncogene, GTPase | Alati | Esineb 7 haiguses |
| L1CAML1 cell adhesion molecule | Alati | Esineb 5 haiguses |
| L2HGDHL-2-hydroxyglutarate dehydrogenase | Alati | Esineb 2 haiguses |
| LAGE3L antigen family member 3 | Alati | Esineb 1 haiguses |
| LAMB1laminin subunit beta 1 | Alati | Esineb 1 haiguses |
| LAS1LLAS1 like ribosome biogenesis factor | Alati | Esineb 2 haiguses |
| LGI3leucine rich repeat LGI family member 3 | Alati | Esineb 1 haiguses |
| LINS1lines homolog 1 | Alati | Esineb 1 haiguses |
| LRRC7leucine rich repeat containing 7 | Alati | Esineb 1 haiguses |
| LSM7LSM7 homolog, U6 small nuclear RNA and mRNA degradation associated | Alati | Esineb 1 haiguses |
| LSSlanosterol synthase | Alati | Esineb 2 haiguses |
| LYRM7LYR motif containing 7 | Alati | Esineb 1 haiguses |
| LZTFL1leucine zipper transcription factor like 1 | Alati | Esineb 2 haiguses |
| MAFMAF bZIP transcription factor | Alati | Esineb 2 haiguses |
| MAGEL2MAGE family member L2 | Alati | Esineb 3 haiguses |
| MAGT1magnesium transporter 1 | Alati | Esineb 1 haiguses |
| MAN1B1mannosidase alpha class 1B member 1 | Alati | Esineb 2 haiguses |
| MANBAmannosidase beta | Alati | Esineb 2 haiguses |
| MAPRE2microtubule associated protein RP/EB family member 2 | Alati | Esineb 2 haiguses |
| MARK2microtubule affinity regulating kinase 2 | Alati | Esineb 1 haiguses |
| MARS1methionyl-tRNA synthetase 1 | Alati | Esineb 1 haiguses |
| MAST1microtubule associated serine/threonine kinase 1 | Alati | Esineb 1 haiguses |
| MAST3microtubule associated serine/threonine kinase 3 | Alati | Esineb 1 haiguses |
| MBD5methyl-CpG binding domain protein 5 | Alati | Esineb 1 haiguses |
| MBOAT7membrane bound acylglycerophosphatidylinositol O-acyltransferase MBOAT7 | Alati | Esineb 1 haiguses |
| MCPH1microcephalin 1 | Alati | Esineb 1 haiguses |
| MDGA2MAM domain containing glycosylphosphatidylinositol anchor 2 | Alati | Esineb 2 haiguses |
| MECP2methyl-CpG binding protein 2 | Alati | Esineb 4 haiguses |
| MED12mediator complex subunit 12 | Alati | Esineb 5 haiguses |
| MED12Lmediator complex subunit 12L | Alati | Esineb 1 haiguses |
| MED16mediator complex subunit 16 | Alati | Esineb 1 haiguses |
| MED23mediator complex subunit 23 | Alati | Esineb 1 haiguses |
| MED27mediator complex subunit 27 | Alati | Esineb 1 haiguses |
| MEIS2Meis homeobox 2 | Alati | Esineb 2 haiguses |
| METTL23methyltransferase 23, arginine | Alati | Esineb 1 haiguses |
| MID2midline 2 | Alati | Esineb 1 haiguses |
| MKRN3makorin ring finger protein 3 | Alati | Esineb 1 haiguses |
| MKS1MKS transition zone complex subunit 1 | Alati | Esineb 5 haiguses |
| MOCS3molybdenum cofactor synthesis 3 | Alati | Esineb 1 haiguses |
| MPLKIPM-phase specific PLK1 interacting protein | Alati | Esineb 1 haiguses |
| MRPS2mitochondrial ribosomal protein S2 | Alati | Esineb 1 haiguses |
| MSL3MSL complex subunit 3 | Alati | Esineb 1 haiguses |
| MTORmechanistic target of rapamycin kinase | Alati | Esineb 3 haiguses |
| MYCNMYCN proto-oncogene, bHLH transcription factor | Alati | Esineb 3 haiguses |
| MYT1Lmyelin transcription factor 1 like | Alati | Esineb 2 haiguses |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Alati | Esineb 2 haiguses |
| NAA15N-alpha-acetyltransferase 15, NatA auxiliary subunit | Alati | Esineb 1 haiguses |
| NAA20N-alpha-acetyltransferase 20, NatB catalytic subunit | Alati | Esineb 1 haiguses |
| NACC1nucleus accumbens associated 1 | Alati | Esineb 1 haiguses |
| NAGLUN-acetyl-alpha-glucosaminidase | Alati | Esineb 1 haiguses |
| NARS1asparaginyl-tRNA synthetase 1 | Alati | Esineb 2 haiguses |
| NCDNneurochondrin | Alati | Esineb 1 haiguses |
| NDST1N-deacetylase and N-sulfotransferase 1 | Alati | Esineb 1 haiguses |
| NDUFA2NADH:ubiquinone oxidoreductase subunit A2 | Alati | Esineb 1 haiguses |
| NEXMIFneurite extension and migration factor | Alati | Esineb 3 haiguses |
| NFIBnuclear factor I B | Alati | Esineb 1 haiguses |
| NFIXnuclear factor I X | Alati | Esineb 3 haiguses |
| NGLY1N-glycanase 1 | Alati | Esineb 2 haiguses |
| NONOnon-POU domain containing octamer binding | Alati | Esineb 1 haiguses |
| NOS3nitric oxide synthase 3 | Alati | Esineb 1 haiguses |
| NOVA2NOVA alternative splicing regulator 2 | Alati | Esineb 1 haiguses |
| NPAP1nuclear pore associated protein 1 | Alati | Esineb 1 haiguses |
| NPC1NPC intracellular cholesterol transporter 1 | Alati | Esineb 1 haiguses |
| NR2F1nuclear receptor subfamily 2 group F member 1 | Alati | Esineb 2 haiguses |
| NSD2nuclear receptor binding SET domain protein 2 | Alati | Esineb 1 haiguses |
| NSUN2NOP2/Sun RNA methyltransferase 2 | Alati | Esineb 1 haiguses |
| NSUN6NOP2/Sun RNA methyltransferase 6 | Alati | Esineb 1 haiguses |
| NTRK1neurotrophic receptor tyrosine kinase 1 | Alati | Esineb 2 haiguses |
| NUP107nucleoporin 107 | Alati | Esineb 1 haiguses |
| NUP37nucleoporin 37 | Alati | Esineb 1 haiguses |
| NUS1NUS1 dehydrodolichyl diphosphate synthase subunit | Alati | Esineb 2 haiguses |
| OGTO-linked N-acetylglucosamine (GlcNAc) transferase | Alati | Esineb 1 haiguses |
| OPHN1oligophrenin 1 | Alati | Esineb 2 haiguses |
| OTUD5OTU deubiquitinase 5 | Alati | Esineb 1 haiguses |
| OXR1oxidation resistance 1 | Alati | Esineb 1 haiguses |
| PACS2phosphofurin acidic cluster sorting protein 2 | Alati | Esineb 2 haiguses |
| PAK3p21 (RAC1) activated kinase 3 | Alati | Esineb 1 haiguses |
| PCYT2phosphate cytidylyltransferase 2, ethanolamine | Alati | Esineb 1 haiguses |
| PDCD6IPprogrammed cell death 6 interacting protein | Alati | Esineb 1 haiguses |
| PDE4Dphosphodiesterase 4D | Alati | Esineb 3 haiguses |
| PDHA1pyruvate dehydrogenase E1 subunit alpha 1 | Alati | Esineb 1 haiguses |
| PDZD8PDZ domain containing 8 | Alati | Esineb 1 haiguses |
| PEX11Bperoxisomal biogenesis factor 11 beta | Alati | Esineb 1 haiguses |
| PEX12peroxisomal biogenesis factor 12 | Alati | Esineb 1 haiguses |
| PGM2L1phosphoglucomutase 2 like 1 | Alati | Esineb 1 haiguses |
| PHACTR1phosphatase and actin regulator 1 | Alati | Esineb 1 haiguses |
| PHF21APHD finger protein 21A | Alati | Esineb 2 haiguses |
| PHF8PHD finger protein 8 | Alati | Esineb 1 haiguses |
| PHIPPHIP subunit of CUL4-Ring ligase complex | Alati | Esineb 2 haiguses |
| PI4KAphosphatidylinositol 4-kinase alpha | Alati | Esineb 2 haiguses |
| PIEZO2piezo type mechanosensitive ion channel component 2 | Alati | Esineb 2 haiguses |
| PIGBphosphatidylinositol glycan anchor biosynthesis class B | Alati | Esineb 1 haiguses |
| PIGCphosphatidylinositol glycan anchor biosynthesis class C | Alati | Esineb 1 haiguses |
| PIGLphosphatidylinositol glycan anchor biosynthesis class L | Alati | Esineb 3 haiguses |
| PIGOphosphatidylinositol glycan anchor biosynthesis class O | Alati | Esineb 2 haiguses |
| PIGTphosphatidylinositol glycan anchor biosynthesis class T | Alati | Esineb 1 haiguses |
| PIGVphosphatidylinositol glycan anchor biosynthesis class V | Alati | Esineb 2 haiguses |
| PLK4polo like kinase 4 | Alati | Esineb 3 haiguses |
| PLP1proteolipid protein 1 | Alati | Esineb 3 haiguses |
| PNPLA6patatin like domain 6, lysophospholipase | Alati | Esineb 4 haiguses |
| POLA1DNA polymerase alpha 1, catalytic subunit | Alati | Esineb 2 haiguses |
| POLR1ARNA polymerase I subunit A | Alati | Esineb 1 haiguses |
| POLR3BRNA polymerase III subunit B | Alati | Esineb 2 haiguses |
| POMT1protein O-mannosyltransferase 1 | Alati | Esineb 5 haiguses |
| POU3F3POU class 3 homeobox 3 | Alati | Esineb 1 haiguses |
| PPFIA3PPFI scaffold protein A3 | Alati | Esineb 1 haiguses |
| PPOXprotoporphyrinogen oxidase | Alati | Esineb 1 haiguses |
| PPP2R1Aprotein phosphatase 2 scaffold subunit Aalpha | Alati | Esineb 2 haiguses |
| PPP2R5Dprotein phosphatase 2 regulatory subunit B'delta | Alati | Esineb 1 haiguses |
| PPP3CAprotein phosphatase 3 catalytic subunit alpha | Alati | Esineb 3 haiguses |
| PRDM13PR/SET domain 13 | Alati | Esineb 1 haiguses |
| PRODHproline dehydrogenase 1 | Alati | Esineb 1 haiguses |
| PRR12proline rich 12 | Alati | Esineb 1 haiguses |
| PSMD12proteasome 26S subunit, non-ATPase 12 | Alati | Esineb 1 haiguses |
| PSPHphosphoserine phosphatase | Alati | Esineb 1 haiguses |
| PTDSS1phosphatidylserine synthase 1 | Alati | Esineb 2 haiguses |
| PTPAprotein phosphatase 2 phosphatase activator | Alati | Esineb 1 haiguses |
| PTRHD1peptidyl-tRNA hydrolase domain containing 1 | Alati | Esineb 1 haiguses |
| PUM1pumilio RNA binding family member 1 | Alati | Esineb 1 haiguses |
| PUS7pseudouridine synthase 7 | Alati | Esineb 1 haiguses |
| PWAR1Prader Willi/Angelman region RNA 1 | Alati | Esineb 1 haiguses |
| PWRN1Prader-Willi region non-protein coding RNA 1 | Alati | Esineb 1 haiguses |
| QRICH1glutamine rich 1 | Alati | Esineb 1 haiguses |
| RAB11BRAB11B, member RAS oncogene family | Alati | Esineb 1 haiguses |
| RAB39BRAB39B, member RAS oncogene family | Alati | Esineb 2 haiguses |
| RAC1Rac family small GTPase 1 | Alati | Esineb 2 haiguses |
| RAD50RAD50 double strand break repair protein | Alati | Esineb 1 haiguses |
| RAD51RAD51 recombinase | Alati | Esineb 2 haiguses |
| RAI1retinoic acid induced 1 | Alati | Esineb 2 haiguses |
| RALARAS like proto-oncogene A | Alati | Esineb 1 haiguses |
| RAP1GDS1Rap1 GTPase-GDP dissociation stimulator 1 | Alati | Esineb 1 haiguses |
| RARBretinoic acid receptor beta | Alati | Esineb 1 haiguses |
| RBBP8RB binding protein 8, endonuclease | Alati | Esineb 2 haiguses |
| RBM28RNA binding motif protein 28 | Alati | Esineb 2 haiguses |
| RFX7regulatory factor X7 | Alati | Esineb 1 haiguses |
| RHOBTB2Rho related BTB domain containing 2 | Alati | Esineb 3 haiguses |
| RIC1RIC1 partner of RAB6A GEF complex | Alati | Esineb 1 haiguses |
| RLIMring finger protein, LIM domain interacting | Alati | Esineb 1 haiguses |
| RNU2-2RNA, U2 small nuclear 2 | Alati | Esineb 1 haiguses |
| RNU4-2RNA, U4 small nuclear 2 | Alati | Esineb 1 haiguses |
| RPL10ribosomal protein L10 | Alati | Esineb 1 haiguses |
| RPS6KA3ribosomal protein S6 kinase A3 | Alati | Esineb 3 haiguses |
| RRP7Aribosomal RNA processing 7 homolog A | Alati | Esineb 1 haiguses |
| RSPRY1ring finger and SPRY domain containing 1 | Alati | Esineb 2 haiguses |
| RSRC1arginine and serine rich coiled-coil 1 | Alati | Esineb 1 haiguses |
| RUBCNrubicon autophagy regulator | Alati | Esineb 2 haiguses |
| RUSC2RUN and SH3 domain containing 2 | Alati | Esineb 1 haiguses |
| SCAF4SR-related CTD associated factor 4 | Alati | Esineb 1 haiguses |
| SCAPERS-phase cyclin A associated protein in the ER | Alati | Esineb 2 haiguses |
| SCN8Asodium voltage-gated channel alpha subunit 8 | Alati | Esineb 4 haiguses |
| SDCCAG8SHH signaling and ciliogenesis regulator SDCCAG8 | Alati | Esineb 2 haiguses |
| SERAC1serine active site containing 1 | Alati | Esineb 2 haiguses |
| SETD2SET domain containing 2, histone lysine methyltransferase | Alati | Esineb 3 haiguses |
| SETD5SET domain containing 5 | Alati | Esineb 1 haiguses |
| SLC13A1solute carrier family 13 member 1 | Alati | Esineb 1 haiguses |
| SLC2A1solute carrier family 2 member 1 | Alati | Esineb 9 haiguses |
| SLC32A1solute carrier family 32 member 1 | Alati | Esineb 2 haiguses |
| SLC38A3solute carrier family 38 member 3 | Alati | Esineb 2 haiguses |
| SLC39A8solute carrier family 39 member 8 | Alati | Esineb 1 haiguses |
| SLC4A4solute carrier family 4 member 4 | Alati | Esineb 1 haiguses |
| SLC6A1solute carrier family 6 member 1 | Alati | Esineb 2 haiguses |
| SLC6A19solute carrier family 6 member 19 | Alati | Esineb 2 haiguses |
| SLC6A8solute carrier family 6 member 8 | Alati | Esineb 2 haiguses |
| SLITRK2SLIT and NTRK like family member 2 | Alati | Esineb 1 haiguses |
| SMARCA2SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 | Alati | Esineb 3 haiguses |
| SMARCA4SWI/SNF related BAF chromatin remodeling complex subunit ATPase 4 | Alati | Esineb 1 haiguses |
| SMARCC2SWI/SNF related BAF chromatin remodeling complex subunit C2 | Alati | Esineb 1 haiguses |
| SMARCD1SWI/SNF related BAF chromatin remodeling complex subunit D1 | Alati | Esineb 1 haiguses |
| SMC3structural maintenance of chromosomes 3 | Alati | Esineb 2 haiguses |
| SMG9SMG9 nonsense mediated mRNA decay factor | Alati | Esineb 1 haiguses |
| SMSspermine synthase | Alati | Esineb 1 haiguses |
| SNF8SNF8 subunit of ESCRT-II | Alati | Esineb 1 haiguses |
| SNORD115-1small nucleolar RNA, C/D box 115-1 | Alati | Esineb 1 haiguses |
| SNORD116-1small nucleolar RNA, C/D box 116-1 | Alati | Esineb 1 haiguses |
| SNX14sorting nexin 14 | Alati | Esineb 1 haiguses |
| SONSON DNA and RNA binding protein | Alati | Esineb 2 haiguses |
| SOX10SRY-box transcription factor 10 | Alati | Esineb 3 haiguses |
| SOX4SRY-box transcription factor 4 | Alati | Esineb 1 haiguses |
| SOX5SRY-box transcription factor 5 | Alati | Esineb 2 haiguses |
| SPENspen family transcriptional repressor | Alati | Esineb 2 haiguses |
| SPOPspeckle type BTB/POZ protein | Alati | Esineb 2 haiguses |
| SPOUT1SPOUT domain containing methyltransferase 1 | Alati | Esineb 1 haiguses |
| SPTSSAserine palmitoyltransferase small subunit A | Alati | Esineb 1 haiguses |
| SRD5A3steroid 5 alpha-reductase 3 | Alati | Esineb 2 haiguses |
| SSR4signal sequence receptor subunit 4 | Alati | Esineb 2 haiguses |
| STAG1STAG1 cohesin complex component | Alati | Esineb 2 haiguses |
| STEEP1STING1 ER exit protein 1 | Alati | Esineb 1 haiguses |
| STILSTIL centriolar assembly protein | Alati | Esineb 6 haiguses |
| STT3ASTT3 oligosaccharyltransferase complex catalytic subunit A | Alati | Esineb 3 haiguses |
| STT3BSTT3 oligosaccharyltransferase complex catalytic subunit B | Alati | Esineb 2 haiguses |
| SUPT16HSPT16 homolog, facilitates chromatin remodeling subunit | Alati | Esineb 2 haiguses |
| SVBPsmall vasohibin binding protein | Alati | Esineb 1 haiguses |
| SYPsynaptophysin | Alati | Esineb 1 haiguses |
| TACO1translational activator of cytochrome c oxidase I | Alati | Esineb 2 haiguses |
| TAF2TATA-box binding protein associated factor 2 | Alati | Esineb 2 haiguses |
| TAF6TATA-box binding protein associated factor 6 | Alati | Esineb 1 haiguses |
| TAF8TATA-box binding protein associated factor 8 | Alati | Esineb 1 haiguses |
| TANGO2transport and golgi organization 2 homolog | Alati | Esineb 2 haiguses |
| TBC1D24TBC1 domain family member 24 | Alati | Esineb 3 haiguses |
| TBCDtubulin folding cofactor D | Alati | Esineb 1 haiguses |
| TBCEtubulin folding cofactor E | Alati | Esineb 4 haiguses |
| TBL1XR1TBL1X/Y related 1 | Alati | Esineb 3 haiguses |
| TCEAL1transcription elongation factor A like 1 | Alati | Esineb 1 haiguses |
| TECPR2tectonin beta-propeller repeat containing 2 | Alati | Esineb 2 haiguses |
| TECRtrans-2,3-enoyl-CoA reductase | Alati | Esineb 1 haiguses |
| TELO2telomere maintenance 2 | Alati | Esineb 1 haiguses |
| TFE3transcription factor binding to IGHM enhancer 3 | Alati | Esineb 1 haiguses |
| THOC6THO complex subunit 6 | Alati | Esineb 1 haiguses |
| THUMPD1THUMP domain 1 NAT10 acetyltransferase adaptor | Alati | Esineb 1 haiguses |
| TIAM1TIAM Rac1 associated GEF 1 | Alati | Esineb 1 haiguses |
| TLK2tousled like kinase 2 | Alati | Esineb 1 haiguses |
| TMEM147transmembrane protein 147 | Alati | Esineb 1 haiguses |
| TMEM216transmembrane protein 216 | Alati | Esineb 3 haiguses |
| TMEM67transmembrane protein 67 | Alati | Esineb 3 haiguses |
| TMLHEtrimethyllysine hydroxylase, epsilon | Alati | Esineb 1 haiguses |
| TMTC3transmembrane O-mannosyltransferase targeting cadherins 3 | Alati | Esineb 1 haiguses |
| TNIKTRAF2 and NCK interacting kinase | Alati | Esineb 1 haiguses |
| TNPO2transportin 2 | Alati | Esineb 1 haiguses |
| TNRC6Btrinucleotide repeat containing adaptor 6B | Alati | Esineb 1 haiguses |
| TOE1target of EGR1, exonuclease | Alati | Esineb 2 haiguses |
| TP53tumor protein p53 | Alati | Esineb 1 haiguses |
| TPRKBTP53RK binding protein | Alati | Esineb 1 haiguses |
| TRA2Btransformer 2 beta homolog | Alati | Esineb 1 haiguses |
| TRAPPC14trafficking protein particle complex subunit 14 | Alati | Esineb 1 haiguses |
| TRAPPC9trafficking protein particle complex subunit 9 | Alati | Esineb 1 haiguses |
| TRIOtrio Rho guanine nucleotide exchange factor | Alati | Esineb 2 haiguses |
| TRIP12thyroid hormone receptor interactor 12 | Alati | Esineb 1 haiguses |
| TRMT10AtRNA methyltransferase 10A | Alati | Esineb 2 haiguses |
| TRPM3transient receptor potential cation channel subfamily M member 3 | Alati | Esineb 1 haiguses |
| TSEN15tRNA splicing endonuclease subunit 15 | Alati | Esineb 1 haiguses |
| TSHRthyroid stimulating hormone receptor | Alati | Esineb 1 haiguses |
| TSPAN7tetraspanin 7 | Alati | Esineb 1 haiguses |
| TTC5tetratricopeptide repeat domain 5 | Alati | Esineb 1 haiguses |
| TTI1TELO2 interacting protein 1 | Alati | Esineb 1 haiguses |
| TUBBtubulin beta class I | Alati | Esineb 2 haiguses |
| TUBB2Btubulin beta 2B class IIb | Alati | Esineb 4 haiguses |
| TUBB3tubulin beta 3 class III | Alati | Esineb 3 haiguses |
| TUSC3tumor suppressor candidate 3 | Alati | Esineb 1 haiguses |
| UBE2Aubiquitin conjugating enzyme E2 A | Alati | Esineb 1 haiguses |
| UBR7ubiquitin protein ligase E3 component n-recognin 7 | Alati | Esineb 1 haiguses |
| UFSP2UFM1 specific peptidase 2 | Alati | Esineb 2 haiguses |
| UNC13Aunc-13 homolog A | Alati | Esineb 1 haiguses |
| USP7ubiquitin specific peptidase 7 | Alati | Esineb 2 haiguses |
| USP9Xubiquitin specific peptidase 9 X-linked | Alati | Esineb 2 haiguses |
| VAMP2vesicle associated membrane protein 2 | Alati | Esineb 1 haiguses |
| VARS1valyl-tRNA synthetase 1 | Alati | Esineb 1 haiguses |
| VLDLRvery low density lipoprotein receptor | Alati | Esineb 2 haiguses |
| VPS13Bvacuolar protein sorting 13 homolog B | Alati | Esineb 2 haiguses |
| VPS35LVPS35 endosomal protein sorting factor like | Alati | Esineb 2 haiguses |
| VPS53VPS53 subunit of GARP complex | Alati | Esineb 1 haiguses |
| WARS1tryptophanyl-tRNA synthetase 1 | Alati | Esineb 1 haiguses |
| WARS2tryptophanyl tRNA synthetase 2, mitochondrial | Alati | Esineb 3 haiguses |
| WASHC4WASH complex subunit 4 | Alati | Esineb 1 haiguses |
| WBP4WW domain binding protein 4 | Alati | Esineb 1 haiguses |
| WDFY3WD repeat and FYVE domain containing 3 | Alati | Esineb 1 haiguses |
| WDR26WD repeat domain 26 | Alati | Esineb 2 haiguses |
| WDR37WD repeat domain 37 | Alati | Esineb 1 haiguses |
| WDR4WDR4 tRNA N7-guanosine methyltransferase non-catalytic subunit | Alati | Esineb 1 haiguses |
| WDR62WD repeat domain 62 | Alati | Esineb 1 haiguses |
| WDR73WD repeat domain 73 | Alati | Esineb 2 haiguses |
| WDR83OSWD repeat domain 83 opposite strand | Alati | Esineb 1 haiguses |
| WSB2WD repeat and SOCS box containing 2 | Alati | Esineb 1 haiguses |
| WWOXWW domain containing oxidoreductase | Alati | Esineb 1 haiguses |
| YAP1Yes1 associated transcriptional regulator | Alati | Esineb 2 haiguses |
| YME1L1YME1 like 1 ATPase | Alati | Esineb 1 haiguses |
| YWHAGtyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma | Alati | Esineb 2 haiguses |
| YWHAZtyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta | Alati | Esineb 1 haiguses |
| YY1YY1 transcription factor | Alati | Esineb 1 haiguses |
| ZBTB24zinc finger and BTB domain containing 24 | Alati | Esineb 2 haiguses |
| ZBTB7Azinc finger and BTB domain containing 7A | Alati | Esineb 1 haiguses |
| ZC3H14zinc finger CCCH-type containing 14 | Alati | Esineb 1 haiguses |
| ZDHHC9zDHHC palmitoyltransferase 9 | Alati | Esineb 2 haiguses |
| ZFXzinc finger protein X-linked | Alati | Esineb 1 haiguses |
| ZIC1Zic family zinc finger 1 | Alati | Esineb 3 haiguses |
| ZMIZ1zinc finger MIZ-type containing 1 | Alati | Esineb 1 haiguses |
| ZNF668zinc finger protein 668 | Alati | Esineb 1 haiguses |
| ZNF711ZFX family zinc finger ZNF711 | Alati | Esineb 1 haiguses |
| ZSWIM6zinc finger SWIM-type containing 6 | Alati | Esineb 3 haiguses |
| ACDACD shelterin complex subunit and telomerase recruitment factor | Väga sageli (80–99%) | Esineb 1 haiguses |
| ACTBactin beta | Väga sageli (80–99%) | Esineb 3 haiguses |
| ADAMTS3ADAM metallopeptidase with thrombospondin type 1 motif 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ADSLadenylosuccinate lyase | Väga sageli (80–99%) | Esineb 2 haiguses |
| AFF4ALF transcription elongation factor 4 | Väga sageli (80–99%) | Esineb 2 haiguses |
| AGAaspartylglucosaminidase | Väga sageli (80–99%) | Esineb 2 haiguses |
| AHSGalpha 2-HS glycoprotein | Väga sageli (80–99%) | Esineb 1 haiguses |
| ALDH4A1aldehyde dehydrogenase 4 family member A1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| ALDH5A1aldehyde dehydrogenase 5 family member A1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| ALG1ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Väga sageli (80–99%) | Esineb 1 haiguses |
| ALG11ALG11 alpha-1,2-mannosyltransferase | Väga sageli (80–99%) | Esineb 1 haiguses |
| ALG9ALG9 alpha-1,2-mannosyltransferase | Väga sageli (80–99%) | Esineb 2 haiguses |
| ANK1ankyrin 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| AP1S1adaptor related protein complex 1 subunit sigma 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| APPamyloid beta precursor protein | Väga sageli (80–99%) | Esineb 2 haiguses |
| ARID2AT-rich interaction domain 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ARL3ARF like GTPase 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ATAD3AATPase family AAA domain containing 3A | Väga sageli (80–99%) | Esineb 2 haiguses |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Väga sageli (80–99%) | Esineb 4 haiguses |
| ATP7AATPase copper transporting alpha | Väga sageli (80–99%) | Esineb 3 haiguses |
| ATP7BATPase copper transporting beta | Väga sageli (80–99%) | Esineb 1 haiguses |
| ATRATR checkpoint kinase | Väga sageli (80–99%) | Esineb 2 haiguses |
| ATRIPATR interacting protein | Väga sageli (80–99%) | Esineb 1 haiguses |
| AUTS2activator of transcription and developmental regulator AUTS2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| B3GLCTbeta 3-glucosyltransferase | Väga sageli (80–99%) | Esineb 2 haiguses |
| B4GAT1beta-1,4-glucuronyltransferase 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| B9D2B9 domain containing 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Väga sageli (80–99%) | Esineb 1 haiguses |
| BCRBCR activator of RhoGEF and GTPase | Väga sageli (80–99%) | Esineb 1 haiguses |
| BRD4bromodomain containing 4 | Väga sageli (80–99%) | Esineb 2 haiguses |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Väga sageli (80–99%) | Esineb 1 haiguses |
| CA8carbonic anhydrase 8 (inactive) | Väga sageli (80–99%) | Esineb 1 haiguses |
| CACNA1Ecalcium voltage-gated channel subunit alpha1 E | Väga sageli (80–99%) | Esineb 1 haiguses |
| CACNA1Icalcium voltage-gated channel subunit alpha1 I | Väga sageli (80–99%) | Esineb 1 haiguses |
| CANT1calcium activated nucleotidase 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| CASKcalcium/calmodulin dependent serine protein kinase | Väga sageli (80–99%) | Esineb 2 haiguses |
| CASZ1castor zinc finger 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CBY1chibby 1, beta catenin antagonist | Väga sageli (80–99%) | Esineb 1 haiguses |
| CCBE1collagen and calcium binding EGF domains 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| CCDC22CCC complex scaffolding subunit CCDC22 | Väga sageli (80–99%) | Esineb 2 haiguses |
| CD96CD96 molecule | Väga sageli (80–99%) | Esineb 1 haiguses |
| CDK4cyclin dependent kinase 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CDKL5cyclin dependent kinase like 5 | Väga sageli (80–99%) | Esineb 3 haiguses |
| CENPEcentromere protein E | Väga sageli (80–99%) | Esineb 1 haiguses |
| CEP120centrosomal protein 120 | Väga sageli (80–99%) | Esineb 2 haiguses |
| CEP41centrosomal protein 41 | Väga sageli (80–99%) | Esineb 3 haiguses |
| CKAP2Lcytoskeleton associated protein 2L | Väga sageli (80–99%) | Esineb 2 haiguses |
| CLIP2CAP-Gly domain containing linker protein 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CLN8CLN8 transmembrane ER and ERGIC protein | Väga sageli (80–99%) | Esineb 2 haiguses |
| COL4A1collagen type IV alpha 1 chain | Väga sageli (80–99%) | Esineb 2 haiguses |
| CPAPcentrosome assembly and centriole elongation protein | Väga sageli (80–99%) | Esineb 1 haiguses |
| CPLANE1ciliogenesis and planar polarity effector complex subunit 1 | Väga sageli (80–99%) | Esineb 3 haiguses |
| CRKLCRK like proto-oncogene, adaptor protein | Väga sageli (80–99%) | Esineb 1 haiguses |
| CRPPACDP-L-ribitol pyrophosphorylase A | Väga sageli (80–99%) | Esineb 2 haiguses |
| CSGALNACT1chondroitin sulfate N-acetylgalactosaminyltransferase 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CSNK2A1casein kinase 2 alpha 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CSPP1centrosome and spindle pole associated protein 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| DDB2damage specific DNA binding protein 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| DDHD2DDHD domain containing 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| DGCR2DiGeorge syndrome critical region gene 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| DGCR6DiGeorge syndrome critical region gene 6 | Väga sageli (80–99%) | Esineb 1 haiguses |
| DGCR8DGCR8 microprocessor complex subunit | Väga sageli (80–99%) | Esineb 1 haiguses |
| DHCR2424-dehydrocholesterol reductase | Väga sageli (80–99%) | Esineb 1 haiguses |
| DHCR77-dehydrocholesterol reductase | Väga sageli (80–99%) | Esineb 2 haiguses |
| DIS3L2DIS3 like 3'-5' exoribonuclease 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| DKC1dyskerin pseudouridine synthase 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| DMXL2Dmx like 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Väga sageli (80–99%) | Esineb 1 haiguses |
| DPYDdihydropyrimidine dehydrogenase | Väga sageli (80–99%) | Esineb 2 haiguses |
| DPYSL5dihydropyrimidinase like 5 | Väga sageli (80–99%) | Esineb 1 haiguses |
| DYRK1Adual specificity tyrosine phosphorylation regulated kinase 1A | Väga sageli (80–99%) | Esineb 2 haiguses |
| EBF3EBF transcription factor 3 | Väga sageli (80–99%) | Esineb 2 haiguses |
| EFTUD2elongation factor Tu GTP binding domain containing 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| EHMT1euchromatic histone lysine methyltransferase 1 | Väga sageli (80–99%) | Esineb 3 haiguses |
| EIF4Heukaryotic translation initiation factor 4H | Väga sageli (80–99%) | Esineb 1 haiguses |
| ELMO2engulfment and cell motility 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ELNelastin | Väga sageli (80–99%) | Esineb 2 haiguses |
| EPG5ectopic P-granules 5 autophagy tethering factor | Väga sageli (80–99%) | Esineb 1 haiguses |
| ERCC1ERCC excision repair 1, endonuclease non-catalytic subunit | Väga sageli (80–99%) | Esineb 1 haiguses |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | Väga sageli (80–99%) | Esineb 4 haiguses |
| ERCC3ERCC excision repair 3, TFIIH core complex helicase subunit | Väga sageli (80–99%) | Esineb 3 haiguses |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Väga sageli (80–99%) | Esineb 5 haiguses |
| ERCC5ERCC excision repair 5, endonuclease | Väga sageli (80–99%) | Esineb 2 haiguses |
| ERCC8ERCC excision repair 8, CSA ubiquitin ligase complex subunit | Väga sageli (80–99%) | Esineb 3 haiguses |
| ESS2ess-2 spliceosome associated protein | Väga sageli (80–99%) | Esineb 1 haiguses |
| EZH2enhancer of zeste 2 polycomb repressive complex 2 subunit | Väga sageli (80–99%) | Esineb 2 haiguses |
| FANCBFA complementation group B | Väga sageli (80–99%) | Esineb 3 haiguses |
| FAT4FAT atypical cadherin 4 | Väga sageli (80–99%) | Esineb 2 haiguses |
| FBN1fibrillin 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| FBXW11F-box and WD repeat domain containing 11 | Väga sageli (80–99%) | Esineb 1 haiguses |
| FBXW7F-box and WD repeat domain containing 7 | Väga sageli (80–99%) | Esineb 1 haiguses |
| FGFR1fibroblast growth factor receptor 1 | Väga sageli (80–99%) | Esineb 8 haiguses |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Väga sageli (80–99%) | Esineb 1 haiguses |
| FKRPfukutin related protein | Väga sageli (80–99%) | Esineb 4 haiguses |
| FKTNfukutin | Väga sageli (80–99%) | Esineb 3 haiguses |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Väga sageli (80–99%) | Esineb 2 haiguses |
| FOXE1forkhead box E1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| GABRB3gamma-aminobutyric acid type A receptor subunit beta3 | Väga sageli (80–99%) | Esineb 3 haiguses |
| GABRDgamma-aminobutyric acid type A receptor subunit delta | Väga sageli (80–99%) | Esineb 2 haiguses |
| GBE11,4-alpha-glucan branching enzyme 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| GMPPAGDP-mannose pyrophosphorylase A | Väga sageli (80–99%) | Esineb 2 haiguses |
| GNAO1G protein subunit alpha o1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| GORABgolgin, RAB6 interacting | Väga sageli (80–99%) | Esineb 1 haiguses |
| GPC4glypican 4 | Väga sageli (80–99%) | Esineb 2 haiguses |
| GTF2Igeneral transcription factor IIi | Väga sageli (80–99%) | Esineb 1 haiguses |
| GTF2IRD1GTF2I repeat domain containing 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| GTF2IRD2GTF2I repeat domain containing 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| GUSBglucuronidase beta | Väga sageli (80–99%) | Esineb 2 haiguses |
| HBA1hemoglobin subunit alpha 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| HBA2hemoglobin subunit alpha 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| HDAC4histone deacetylase 4 | Väga sageli (80–99%) | Esineb 2 haiguses |
| HDAC8histone deacetylase 8 | Väga sageli (80–99%) | Esineb 3 haiguses |
| HHAThedgehog acyltransferase | Väga sageli (80–99%) | Esineb 1 haiguses |
| HRASHRas proto-oncogene, GTPase | Väga sageli (80–99%) | Esineb 4 haiguses |
| HSPG2heparan sulfate proteoglycan 2 | Väga sageli (80–99%) | Esineb 3 haiguses |
| HYLS1HYLS1 centriolar and ciliogenesis associated | Väga sageli (80–99%) | Esineb 1 haiguses |
| IDUAalpha-L-iduronidase | Väga sageli (80–99%) | Esineb 2 haiguses |
| ITGB6integrin subunit beta 6 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ITPR1inositol 1,4,5-trisphosphate receptor type 1 | Väga sageli (80–99%) | Esineb 3 haiguses |
| KAT6Blysine acetyltransferase 6B | Väga sageli (80–99%) | Esineb 3 haiguses |
| KATNB1katanin regulatory subunit B1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| KATNIPkatanin interacting protein | Väga sageli (80–99%) | Esineb 1 haiguses |
| KCNA1potassium voltage-gated channel subfamily A member 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| KCNAB2potassium voltage-gated channel subfamily A regulatory beta subunit 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| KCNJ10potassium inwardly rectifying channel subfamily J member 10 | Väga sageli (80–99%) | Esineb 4 haiguses |
| KCNJ6potassium inwardly rectifying channel subfamily J member 6 | Väga sageli (80–99%) | Esineb 1 haiguses |
| KDM5Clysine demethylase 5C | Väga sageli (80–99%) | Esineb 1 haiguses |
| KIAA0586KIAA0586 | Väga sageli (80–99%) | Esineb 1 haiguses |
| KIAA0753KIAA0753 | Väga sageli (80–99%) | Esineb 2 haiguses |
| KIF7kinesin family member 7 | Väga sageli (80–99%) | Esineb 3 haiguses |
| KMT2Dlysine methyltransferase 2D | Väga sageli (80–99%) | Esineb 2 haiguses |
| KPTNkaptin, actin binding protein | Väga sageli (80–99%) | Esineb 2 haiguses |
| LAMP2lysosome associated membrane protein 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| LARGE1LARGE xylosyl- and glucuronyltransferase 1 | Väga sageli (80–99%) | Esineb 3 haiguses |
| LETM1leucine zipper and EF-hand containing transmembrane protein 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| LGI1leucine rich glioma inactivated 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| LIMK1LIM domain kinase 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| LRP2LDL receptor related protein 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| LUZP1leucine zipper protein 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| LYSTlysosomal trafficking regulator | Väga sageli (80–99%) | Esineb 3 haiguses |
| MAGmyelin associated glycoprotein | Väga sageli (80–99%) | Esineb 1 haiguses |
| MAN2B1mannosidase alpha class 2B member 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| MAP2K1mitogen-activated protein kinase kinase 1 | Väga sageli (80–99%) | Esineb 4 haiguses |
| MAP2K2mitogen-activated protein kinase kinase 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| MAPK1mitogen-activated protein kinase 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| MAPK10mitogen-activated protein kinase 10 | Väga sageli (80–99%) | Esineb 1 haiguses |
| MAU2MAU2 sister chromatid cohesion factor | Väga sageli (80–99%) | Esineb 1 haiguses |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| MCOLN1mucolipin TRP cation channel 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| MEGF8multiple EGF like domains 8 | Väga sageli (80–99%) | Esineb 1 haiguses |
| METTL27methyltransferase like 27 | Väga sageli (80–99%) | Esineb 1 haiguses |
| MIR17HGmiR-17-92a-1 cluster host gene | Väga sageli (80–99%) | Esineb 1 haiguses |
| MKKSMKKS centrosomal shuttling protein | Väga sageli (80–99%) | Esineb 3 haiguses |
| MLYCDmalonyl-CoA decarboxylase | Väga sageli (80–99%) | Esineb 1 haiguses |
| MMACHCmetabolism of cobalamin associated C | Väga sageli (80–99%) | Esineb 2 haiguses |
| MMADHCmetabolism of cobalamin associated D | Väga sageli (80–99%) | Esineb 2 haiguses |
| MMP23Bmatrix metallopeptidase 23B | Väga sageli (80–99%) | Esineb 1 haiguses |
| MN1MN1 proto-oncogene, transcriptional regulator | Väga sageli (80–99%) | Esineb 1 haiguses |
| MORC2MORC family CW-type zinc finger 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| MSL2MSL complex subunit 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| MVKmevalonate kinase | Väga sageli (80–99%) | Esineb 1 haiguses |
| MYO5Amyosin VA | Väga sageli (80–99%) | Esineb 3 haiguses |
| NAGAalpha-N-acetylgalactosaminidase | Väga sageli (80–99%) | Esineb 1 haiguses |
| NCF1neutrophil cytosolic factor 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| NDE1nudE neurodevelopment protein 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| NEUROD2neuronal differentiation 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| NINninein | Väga sageli (80–99%) | Esineb 1 haiguses |
| NIPBLNIPBL cohesin loading factor | Väga sageli (80–99%) | Esineb 2 haiguses |
| NPHP1nephrocystin 1 | Väga sageli (80–99%) | Esineb 3 haiguses |
| NR4A2nuclear receptor subfamily 4 group A member 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| NRASNRAS proto-oncogene, GTPase | Väga sageli (80–99%) | Esineb 3 haiguses |
| NSD1nuclear receptor binding SET domain protein 1 | Väga sageli (80–99%) | Esineb 3 haiguses |
| NSDHLNAD(P) dependent 3-beta-hydroxysteroid dehydrogenase NSDHL | Väga sageli (80–99%) | Esineb 2 haiguses |
| NSMCE2NSE2 SUMO ligase component of SMC5/6 complex | Väga sageli (80–99%) | Esineb 1 haiguses |
| NT5C25'-nucleotidase, cytosolic II | Väga sageli (80–99%) | Esineb 2 haiguses |
| NTNG1netrin G1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| NUP85nucleoporin 85 | Väga sageli (80–99%) | Esineb 1 haiguses |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Väga sageli (80–99%) | Esineb 2 haiguses |
| OFD1OFD1 centriole and centriolar satellite protein | Väga sageli (80–99%) | Esineb 4 haiguses |
| PACS1phosphofurin acidic cluster sorting protein 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| PARNpoly(A)-specific ribonuclease | Väga sageli (80–99%) | Esineb 1 haiguses |
| PAX6paired box 6 | Väga sageli (80–99%) | Esineb 3 haiguses |
| PCDHGC4protocadherin gamma subfamily C, 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PCNTpericentrin | Väga sageli (80–99%) | Esineb 3 haiguses |
| PDE6Dphosphodiesterase 6D | Väga sageli (80–99%) | Esineb 2 haiguses |
| PDPNpodoplanin | Väga sageli (80–99%) | Esineb 1 haiguses |
| PEX1peroxisomal biogenesis factor 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| PEX6peroxisomal biogenesis factor 6 | Väga sageli (80–99%) | Esineb 2 haiguses |
| PHF6PHD finger protein 6 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PIBF1progesterone immunomodulatory binding factor 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PIDD1p53-induced death domain protein 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PIGNphosphatidylinositol glycan anchor biosynthesis class N | Väga sageli (80–99%) | Esineb 2 haiguses |
| PIGPphosphatidylinositol glycan anchor biosynthesis class P | Väga sageli (80–99%) | Esineb 1 haiguses |
| PIGQphosphatidylinositol glycan anchor biosynthesis class Q | Väga sageli (80–99%) | Esineb 1 haiguses |
| PMPCApeptidase, mitochondrial processing subunit alpha | Väga sageli (80–99%) | Esineb 2 haiguses |
| PNKPpolynucleotide kinase 3'-phosphatase | Väga sageli (80–99%) | Esineb 1 haiguses |
| POGZpogo transposable element derived with ZNF domain | Väga sageli (80–99%) | Esineb 2 haiguses |
| POMGNT1protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | Väga sageli (80–99%) | Esineb 2 haiguses |
| POMGNT2protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-) | Väga sageli (80–99%) | Esineb 2 haiguses |
| POMKprotein O-mannose kinase | Väga sageli (80–99%) | Esineb 1 haiguses |
| POMT2protein O-mannosyltransferase 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| PPFIBP1PPFIB scaffold protein 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PPM1Dprotein phosphatase, Mg2+/Mn2+ dependent 1D | Väga sageli (80–99%) | Esineb 1 haiguses |
| PPP1R15Bprotein phosphatase 1 regulatory subunit 15B | Väga sageli (80–99%) | Esineb 2 haiguses |
| PQBP1polyglutamine binding protein 1 | Väga sageli (80–99%) | Esineb 3 haiguses |
| PRDM16PR/SET domain 16 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Väga sageli (80–99%) | Esineb 2 haiguses |
| PRKCZprotein kinase C zeta | Väga sageli (80–99%) | Esineb 1 haiguses |
| PRMT7protein arginine methyltransferase 7 | Väga sageli (80–99%) | Esineb 2 haiguses |
| PSMC3proteasome 26S subunit, ATPase 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PTCH1patched 1 | Väga sageli (80–99%) | Esineb 9 haiguses |
| PTENphosphatase and tensin homolog | Väga sageli (80–99%) | Esineb 7 haiguses |
| PUF60poly(U) binding splicing factor 60 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PYCR1pyrroline-5-carboxylate reductase 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| PYCR2pyrroline-5-carboxylate reductase 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| QDPRquinoid dihydropteridine reductase | Väga sageli (80–99%) | Esineb 2 haiguses |
| RAB23RAB23, member RAS oncogene family | Väga sageli (80–99%) | Esineb 2 haiguses |
| RAB3GAP1RAB3 GTPase activating protein catalytic subunit 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| RAB3GAP2RAB3 GTPase activating non-catalytic protein subunit 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| RAD21RAD21 cohesin complex component | Väga sageli (80–99%) | Esineb 2 haiguses |
| RB1RB transcriptional corepressor 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| RELNreelin | Väga sageli (80–99%) | Esineb 2 haiguses |
| REREarginine-glutamic acid dipeptide repeats | Väga sageli (80–99%) | Esineb 2 haiguses |
| RFC2replication factor C subunit 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| RNF125ring finger protein 125 | Väga sageli (80–99%) | Esineb 1 haiguses |
| RNU4ATACRNA, U4atac small nuclear | Väga sageli (80–99%) | Esineb 3 haiguses |
| ROBO1roundabout guidance receptor 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| RPGRIP1LRPGRIP1 like | Väga sageli (80–99%) | Esineb 2 haiguses |
| RTEL1regulator of telomere elongation helicase 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| RXYLT1ribitol xylosyltransferase 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SATB1SATB homeobox 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SATB2SATB homeobox 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Väga sageli (80–99%) | Esineb 4 haiguses |
| SCN1Bsodium voltage-gated channel beta subunit 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SETD1ASET domain containing 1A, histone lysine methyltransferase | Väga sageli (80–99%) | Esineb 1 haiguses |
| SGSM3small G protein signaling modulator 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SHOC2SHOC2 leucine rich repeat scaffold protein | Väga sageli (80–99%) | Esineb 2 haiguses |
| SIK1salt inducible kinase 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SIL1SIL1 nucleotide exchange factor | Väga sageli (80–99%) | Esineb 2 haiguses |
| SKISKI proto-oncogene | Väga sageli (80–99%) | Esineb 3 haiguses |
| SLC12A6solute carrier family 12 member 6 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SLC16A2solute carrier family 16 member 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SLC1A4solute carrier family 1 member 4 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SLC25A22solute carrier family 25 member 22 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SLC29A3solute carrier family 29 member 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SLC35A2solute carrier family 35 member A2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SMAD4SMAD family member 4 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SMC1Astructural maintenance of chromosomes 1A | Väga sageli (80–99%) | Esineb 4 haiguses |
| SNAP29synaptosome associated protein 29 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SOSTsclerostin | Väga sageli (80–99%) | Esineb 1 haiguses |
| SOX3SRY-box transcription factor 3 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SOX6SRY-box transcription factor 6 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SP7Sp7 transcription factor | Väga sageli (80–99%) | Esineb 1 haiguses |
| SPTBN1spectrin beta, non-erythrocytic 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| STRA6signaling receptor and transporter of retinol STRA6 | Väga sageli (80–99%) | Esineb 1 haiguses |
| STX1Asyntaxin 1A | Väga sageli (80–99%) | Esineb 1 haiguses |
| SUCLA2succinate-CoA ligase ADP-forming subunit beta | Väga sageli (80–99%) | Esineb 2 haiguses |
| SUFUSUFU negative regulator of hedgehog signaling | Väga sageli (80–99%) | Esineb 3 haiguses |
| SUMF1sulfatase modifying factor 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SUZ12SUZ12 polycomb repressive complex 2 subunit | Väga sageli (80–99%) | Esineb 2 haiguses |
| SYNGAP1synaptic Ras GTPase activating protein 1 | Väga sageli (80–99%) | Esineb 4 haiguses |
| SYT14synaptotagmin 14 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TAF1TATA-box binding protein associated factor 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| TAF4TATA-box binding protein associated factor 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TANC2tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TATtyrosine aminotransferase | Väga sageli (80–99%) | Esineb 2 haiguses |
| TBC1D7TBC1 domain family member 7 | Väga sageli (80–99%) | Esineb 2 haiguses |
| TBL2transducin beta like 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TBR1T-box brain transcription factor 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TBX1T-box transcription factor 1 | Väga sageli (80–99%) | Esineb 4 haiguses |
| TCF4transcription factor 4 | Väga sageli (80–99%) | Esineb 2 haiguses |
| TCIRG1T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TCTN1tectonic family member 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TCTN2tectonic family member 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TCTN3tectonic family member 3 | Väga sageli (80–99%) | Esineb 4 haiguses |
| TDP2tyrosyl-DNA phosphodiesterase 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| TEFMtranscription elongation factor, mitochondrial | Väga sageli (80–99%) | Esineb 1 haiguses |
| TERCtelomerase RNA component | Väga sageli (80–99%) | Esineb 1 haiguses |
| TERTtelomerase reverse transcriptase | Väga sageli (80–99%) | Esineb 1 haiguses |
| TET3tet methylcytosine dioxygenase 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| THOC2THO complex subunit 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TINF2TERF1 interacting nuclear factor 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TMCO1transmembrane and coiled-coil domains 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| TMEM138transmembrane protein 138 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TMEM218transmembrane protein 218 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TMEM231transmembrane protein 231 | Väga sageli (80–99%) | Esineb 2 haiguses |
| TMEM237transmembrane protein 237 | Väga sageli (80–99%) | Esineb 3 haiguses |
| TMEM270transmembrane protein 270 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TNFRSF11ATNF receptor superfamily member 11a | Väga sageli (80–99%) | Esineb 1 haiguses |
| TOGARAM1TOG array regulator of axonemal microtubules 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TRAIPTRAF interacting protein | Väga sageli (80–99%) | Esineb 1 haiguses |
| TRIM8tripartite motif containing 8 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TRRAPtransformation/transcription domain associated protein | Väga sageli (80–99%) | Esineb 1 haiguses |
| TSHZ3teashirt zinc finger homeobox 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| UBAP2Lubiquitin associated protein 2 like | Väga sageli (80–99%) | Esineb 1 haiguses |
| UBE3Aubiquitin protein ligase E3A | Väga sageli (80–99%) | Esineb 3 haiguses |
| UBE3Bubiquitin protein ligase E3B | Väga sageli (80–99%) | Esineb 1 haiguses |
| UBE4Bubiquitination factor E4B | Väga sageli (80–99%) | Esineb 1 haiguses |
| UPF3BUPF3B regulator of nonsense mediated mRNA decay | Väga sageli (80–99%) | Esineb 2 haiguses |
| VPS11VPS11 core subunit of CORVET and HOPS complexes | Väga sageli (80–99%) | Esineb 2 haiguses |
| VPS37DVPS37D subunit of ESCRT-I | Väga sageli (80–99%) | Esineb 1 haiguses |
| VPS41VPS41 subunit of HOPS complex | Väga sageli (80–99%) | Esineb 1 haiguses |
| WACWW domain containing adaptor with coiled-coil | Väga sageli (80–99%) | Esineb 2 haiguses |
| WASHC5WASH complex subunit 5 | Väga sageli (80–99%) | Esineb 1 haiguses |
| WDR81WD repeat domain 81 | Väga sageli (80–99%) | Esineb 2 haiguses |
| WLSWnt ligand secretion mediator | Väga sageli (80–99%) | Esineb 1 haiguses |
| WNT7BWnt family member 7B | Väga sageli (80–99%) | Esineb 1 haiguses |
| XPAXPA, DNA damage recognition and repair factor | Väga sageli (80–99%) | Esineb 2 haiguses |
| XPCXPC complex subunit, DNA damage recognition and repair factor | Väga sageli (80–99%) | Esineb 1 haiguses |
| XYLT1xylosyltransferase 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| ZBTB18zinc finger and BTB domain containing 18 | Väga sageli (80–99%) | Esineb 2 haiguses |
| ZBTB20zinc finger and BTB domain containing 20 | Väga sageli (80–99%) | Esineb 2 haiguses |
| ZEB2zinc finger E-box binding homeobox 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| ZMYM3zinc finger MYM-type containing 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ZNF142zinc finger protein 142 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ZNF423zinc finger protein 423 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ZNF592zinc finger protein 592 | Väga sageli (80–99%) | Esineb 1 haiguses |
| AARS1alanyl-tRNA synthetase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| AASSaminoadipate-semialdehyde synthase | Sageli (30–79%) | Esineb 1 haiguses |
| ABCC8ATP binding cassette subfamily C member 8 | Sageli (30–79%) | Esineb 3 haiguses |
| ACTA2actin alpha 2, smooth muscle | Sageli (30–79%) | Esineb 1 haiguses |
| ADCY3adenylate cyclase 3 | Sageli (30–79%) | Esineb 1 haiguses |
| ADGRL1adhesion G protein-coupled receptor L1 | Sageli (30–79%) | Esineb 1 haiguses |
| ALG12ALG12 alpha-1,6-mannosyltransferase | Sageli (30–79%) | Esineb 1 haiguses |
| ALG2ALG2 alpha-1,3/1,6-mannosyltransferase | Sageli (30–79%) | Esineb 1 haiguses |
| ANO1anoctamin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| AP3B2adaptor related protein complex 3 subunit beta 2 | Sageli (30–79%) | Esineb 1 haiguses |
| AP5Z1adaptor related protein complex 5 subunit zeta 1 | Sageli (30–79%) | Esineb 2 haiguses |
| ARL6ARF like GTPase 6 | Sageli (30–79%) | Esineb 3 haiguses |
| ARSIarylsulfatase family member I | Sageli (30–79%) | Esineb 1 haiguses |
| ASAH1N-acylsphingosine amidohydrolase 1 | Sageli (30–79%) | Esineb 3 haiguses |
| ASCL1achaete-scute family bHLH transcription factor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| ASLargininosuccinate lyase | Sageli (30–79%) | Esineb 2 haiguses |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Sageli (30–79%) | Esineb 4 haiguses |
| ATP5F1AATP synthase F1 subunit alpha | Sageli (30–79%) | Esineb 1 haiguses |
| ATP6V0A2ATPase H+ transporting V0 subunit a2 | Sageli (30–79%) | Esineb 2 haiguses |
| ATXN7L3ataxin 7 like 3 | Sageli (30–79%) | Esineb 1 haiguses |
| B4GALNT1beta-1,4-N-acetyl-galactosaminyltransferase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| BBS1Bardet-Biedl syndrome 1 | Sageli (30–79%) | Esineb 2 haiguses |
| BBS4Bardet-Biedl syndrome 4 | Sageli (30–79%) | Esineb 2 haiguses |
| BBS9Bardet-Biedl syndrome 9 | Sageli (30–79%) | Esineb 2 haiguses |
| BDNFbrain derived neurotrophic factor | Sageli (30–79%) | Esineb 1 haiguses |
| BMPR1Abone morphogenetic protein receptor type 1A | Sageli (30–79%) | Esineb 1 haiguses |
| BRCA1BRCA1 DNA repair associated | Sageli (30–79%) | Esineb 2 haiguses |
| BRCA2BRCA2 DNA repair associated | Sageli (30–79%) | Esineb 1 haiguses |
| BRIP1BRCA1 interacting DNA helicase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| BUB1BBUB1 mitotic checkpoint serine/threonine kinase B | Sageli (30–79%) | Esineb 1 haiguses |
| BUB3BUB3 mitotic checkpoint protein | Sageli (30–79%) | Esineb 1 haiguses |
| BUD13BUD13 spliceosome associated protein | Sageli (30–79%) | Esineb 1 haiguses |
| C2CD3C2 domain containing 3 centriole elongation regulator | Sageli (30–79%) | Esineb 1 haiguses |
| CACNA1Bcalcium voltage-gated channel subunit alpha1 B | Sageli (30–79%) | Esineb 1 haiguses |
| CACNA1Dcalcium voltage-gated channel subunit alpha1 D | Sageli (30–79%) | Esineb 1 haiguses |
| CACNA2D1calcium voltage-gated channel auxiliary subunit alpha2delta 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CAMTA1calmodulin binding transcription activator 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CARS2cysteinyl-tRNA synthetase 2, mitochondrial | Sageli (30–79%) | Esineb 1 haiguses |
| CCDC28Bcoiled-coil domain containing 28B | Sageli (30–79%) | Esineb 1 haiguses |
| CDC42cell division cycle 42 | Sageli (30–79%) | Esineb 2 haiguses |
| CDC42BPBCDC42 binding protein kinase beta | Sageli (30–79%) | Esineb 1 haiguses |
| CDCA7cell division cycle associated 7 | Sageli (30–79%) | Esineb 2 haiguses |
| CDH2cadherin 2 | Sageli (30–79%) | Esineb 1 haiguses |
| CDONcell adhesion associated, oncogene regulated | Sageli (30–79%) | Esineb 7 haiguses |
| CEP83centrosomal protein 83 | Sageli (30–79%) | Esineb 1 haiguses |
| CEP85Lcentrosomal protein 85L | Sageli (30–79%) | Esineb 1 haiguses |
| CHD1chromodomain helicase DNA binding protein 1 | Sageli (30–79%) | Esineb 2 haiguses |
| CHD5chromodomain helicase DNA binding protein 5 | Sageli (30–79%) | Esineb 1 haiguses |
| CHRNA7cholinergic receptor nicotinic alpha 7 subunit | Sageli (30–79%) | Esineb 1 haiguses |
| CHSY1chondroitin sulfate synthase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CLDN1claudin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CLP1cleavage factor polyribonucleotide kinase subunit 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CLPBClpB family mitochondrial disaggregase | Sageli (30–79%) | Esineb 2 haiguses |
| COA8cytochrome c oxidase assembly factor 8 | Sageli (30–79%) | Esineb 2 haiguses |
| COG2component of oligomeric golgi complex 2 | Sageli (30–79%) | Esineb 1 haiguses |
| COG6component of oligomeric golgi complex 6 | Sageli (30–79%) | Esineb 3 haiguses |
| COL3A1collagen type III alpha 1 chain | Sageli (30–79%) | Esineb 1 haiguses |
| COLEC10collectin subfamily member 10 | Sageli (30–79%) | Esineb 2 haiguses |
| COLEC11collectin subfamily member 11 | Sageli (30–79%) | Esineb 2 haiguses |
| COPB2coat protein complex I subunit beta 2 | Sageli (30–79%) | Esineb 1 haiguses |
| COPZ1coat protein complex I subunit zeta 1 | Sageli (30–79%) | Esineb 1 haiguses |
| COX7Bcytochrome c oxidase subunit 7B | Sageli (30–79%) | Esineb 3 haiguses |
| CRIPTOcripto, EGF-CFC family member | Sageli (30–79%) | Esineb 6 haiguses |
| CTBP1C-terminal binding protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CTHcystathionine gamma-lyase | Sageli (30–79%) | Esineb 1 haiguses |
| CUX1cut like homeobox 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CWC27CWC27 spliceosome associated cyclophilin | Sageli (30–79%) | Esineb 2 haiguses |
| CYFIP2cytoplasmic FMR1 interacting protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| CYP27A1cytochrome P450 family 27 subfamily A member 1 | Sageli (30–79%) | Esineb 2 haiguses |
| DAGLAdiacylglycerol lipase alpha | Sageli (30–79%) | Esineb 1 haiguses |
| DALRD3DALR anticodon binding domain containing 3 | Sageli (30–79%) | Esineb 1 haiguses |
| DCAF17DDB1 and CUL4 associated factor 17 | Sageli (30–79%) | Esineb 1 haiguses |
| DCCDCC netrin 1 receptor | Sageli (30–79%) | Esineb 1 haiguses |
| DDCdopa decarboxylase | Sageli (30–79%) | Esineb 1 haiguses |
| DEPDC5DEP domain containing 5, GATOR1 subcomplex subunit | Sageli (30–79%) | Esineb 3 haiguses |
| DHDDSdehydrodolichyl diphosphate synthase subunit | Sageli (30–79%) | Esineb 2 haiguses |
| DIAPH1diaphanous related formin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| DISP1dispatched RND transporter family member 1 | Sageli (30–79%) | Esineb 6 haiguses |
| DLK1delta like non-canonical Notch ligand 1 | Sageli (30–79%) | Esineb 3 haiguses |
| DLL1delta like canonical Notch ligand 1 | Sageli (30–79%) | Esineb 7 haiguses |
| DLX5distal-less homeobox 5 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAJC6DnaJ heat shock protein family (Hsp40) member C6 | Sageli (30–79%) | Esineb 2 haiguses |
| DNMT3BDNA methyltransferase 3 beta | Sageli (30–79%) | Esineb 2 haiguses |
| DOCK7dedicator of cytokinesis 7 | Sageli (30–79%) | Esineb 1 haiguses |
| DPYSdihydropyrimidinase | Sageli (30–79%) | Esineb 2 haiguses |
| DYNC1H1dynein cytoplasmic 1 heavy chain 1 | Sageli (30–79%) | Esineb 1 haiguses |
| EBPEBP cholestenol delta-isomerase | Sageli (30–79%) | Esineb 2 haiguses |
| EEF1A2eukaryotic translation elongation factor 1 alpha 2 | Sageli (30–79%) | Esineb 1 haiguses |
| EFNB1ephrin B1 | Sageli (30–79%) | Esineb 1 haiguses |
| EMILIN1elastin microfibril interfacer 1 | Sageli (30–79%) | Esineb 1 haiguses |
| ESCO2establishment of sister chromatid cohesion N-acetyltransferase 2 | Sageli (30–79%) | Esineb 4 haiguses |
| ETHE1ETHE1 persulfide dioxygenase | Sageli (30–79%) | Esineb 2 haiguses |
| EXT1exostosin glycosyltransferase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| EXTL3exostosin like glycosyltransferase 3 | Sageli (30–79%) | Esineb 2 haiguses |
| FA2Hfatty acid 2-hydroxylase | Sageli (30–79%) | Esineb 2 haiguses |
| FAAP100FA core complex associated protein 100 | Sageli (30–79%) | Esineb 1 haiguses |
| FANCAFA complementation group A | Sageli (30–79%) | Esineb 2 haiguses |
| FANCCFA complementation group C | Sageli (30–79%) | Esineb 2 haiguses |
| FANCD2FA complementation group D2 | Sageli (30–79%) | Esineb 2 haiguses |
| FANCEFA complementation group E | Sageli (30–79%) | Esineb 2 haiguses |
| FANCFFA complementation group F | Sageli (30–79%) | Esineb 1 haiguses |
| FANCGFA complementation group G | Sageli (30–79%) | Esineb 1 haiguses |
| FANCIFA complementation group I | Sageli (30–79%) | Esineb 1 haiguses |
| FANCLFA complementation group L | Sageli (30–79%) | Esineb 1 haiguses |
| FANCMFA complementation group M | Sageli (30–79%) | Esineb 1 haiguses |
| FAR1fatty acyl-CoA reductase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| FBXO22F-box protein 22 | Sageli (30–79%) | Esineb 1 haiguses |
| FGF12fibroblast growth factor 12 | Sageli (30–79%) | Esineb 1 haiguses |
| FGF8fibroblast growth factor 8 | Sageli (30–79%) | Esineb 6 haiguses |
| FGFR2fibroblast growth factor receptor 2 | Sageli (30–79%) | Esineb 8 haiguses |
| FIBPFGF1 intracellular binding protein | Sageli (30–79%) | Esineb 1 haiguses |
| FIG4FIG4 phosphoinositide 5-phosphatase | Sageli (30–79%) | Esineb 1 haiguses |
| FLVCR1FLVCR choline and heme transporter 1 | Sageli (30–79%) | Esineb 2 haiguses |
| FOXG1forkhead box G1 | Sageli (30–79%) | Esineb 1 haiguses |
| FOXH1forkhead box H1 | Sageli (30–79%) | Esineb 6 haiguses |
| FZR1fizzy and cell division cycle 20 related 1 | Sageli (30–79%) | Esineb 1 haiguses |
| GABBR1gamma-aminobutyric acid type B receptor subunit 1 | Sageli (30–79%) | Esineb 1 haiguses |
| GABRA2gamma-aminobutyric acid type A receptor subunit alpha2 | Sageli (30–79%) | Esineb 1 haiguses |
| GABRA3gamma-aminobutyric acid type A receptor subunit alpha3 | Sageli (30–79%) | Esineb 1 haiguses |
| GABRA5gamma-aminobutyric acid type A receptor subunit alpha5 | Sageli (30–79%) | Esineb 1 haiguses |
| GABRB2gamma-aminobutyric acid type A receptor subunit beta2 | Sageli (30–79%) | Esineb 2 haiguses |
| GABRG2gamma-aminobutyric acid type A receptor subunit gamma2 | Sageli (30–79%) | Esineb 2 haiguses |
| GALEUDP-galactose-4-epimerase | Sageli (30–79%) | Esineb 2 haiguses |
| GANgigaxonin | Sageli (30–79%) | Esineb 2 haiguses |
| GAS1growth arrest specific 1 | Sageli (30–79%) | Esineb 6 haiguses |
| GATA6GATA binding protein 6 | Sageli (30–79%) | Esineb 1 haiguses |
| GCKglucokinase | Sageli (30–79%) | Esineb 2 haiguses |
| GKglycerol kinase | Sageli (30–79%) | Esineb 1 haiguses |
| GLI2GLI family zinc finger 2 | Sageli (30–79%) | Esineb 6 haiguses |
| GLYCTKglycerate kinase | Sageli (30–79%) | Esineb 2 haiguses |
| GNAQG protein subunit alpha q | Sageli (30–79%) | Esineb 3 haiguses |
| GNASGNAS complex locus | Sageli (30–79%) | Esineb 6 haiguses |
| GNB2G protein subunit beta 2 | Sageli (30–79%) | Esineb 1 haiguses |
| GRIN2Aglutamate ionotropic receptor NMDA type subunit 2A | Sageli (30–79%) | Esineb 3 haiguses |
| GRIN2Dglutamate ionotropic receptor NMDA type subunit 2D | Sageli (30–79%) | Esineb 1 haiguses |
| GSSglutathione synthetase | Sageli (30–79%) | Esineb 2 haiguses |
| H4C9H4 clustered histone 9 | Sageli (30–79%) | Esineb 1 haiguses |
| HAAO3-hydroxyanthranilate 3,4-dioxygenase | Sageli (30–79%) | Esineb 1 haiguses |
| HACE1HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 | Sageli (30–79%) | Esineb 2 haiguses |
| HELLShelicase, lymphoid specific | Sageli (30–79%) | Esineb 2 haiguses |
| HEPACAMhepatic and glial cell adhesion molecule | Sageli (30–79%) | Esineb 4 haiguses |
| HGSNATheparan-alpha-glucosaminide N-acetyltransferase | Sageli (30–79%) | Esineb 1 haiguses |
| HNF4Ahepatocyte nuclear factor 4 alpha | Sageli (30–79%) | Esineb 1 haiguses |
| HPD4-hydroxyphenylpyruvate dioxygenase | Sageli (30–79%) | Esineb 1 haiguses |
| IBA57iron-sulfur cluster assembly factor IBA57 | Sageli (30–79%) | Esineb 1 haiguses |
| IFNGinterferon gamma | Sageli (30–79%) | Esineb 2 haiguses |
| IFT140intraflagellar transport 140 | Sageli (30–79%) | Esineb 2 haiguses |
| IGF1Rinsulin like growth factor 1 receptor | Sageli (30–79%) | Esineb 2 haiguses |
| INSinsulin | Sageli (30–79%) | Esineb 1 haiguses |
| INSRinsulin receptor | Sageli (30–79%) | Esineb 2 haiguses |
| IPO8importin 8 | Sageli (30–79%) | Esineb 1 haiguses |
| ITGA7integrin subunit alpha 7 | Sageli (30–79%) | Esineb 1 haiguses |
| IVDisovaleryl-CoA dehydrogenase | Sageli (30–79%) | Esineb 1 haiguses |
| JARID2jumonji and AT-rich interaction domain containing 2 | Sageli (30–79%) | Esineb 1 haiguses |
| KCNA2potassium voltage-gated channel subfamily A member 2 | Sageli (30–79%) | Esineb 2 haiguses |
| KCNB1potassium voltage-gated channel subfamily B member 1 | Sageli (30–79%) | Esineb 1 haiguses |
| KCNH1potassium voltage-gated channel subfamily H member 1 | Sageli (30–79%) | Esineb 2 haiguses |
| KCNH5potassium voltage-gated channel subfamily H member 5 | Sageli (30–79%) | Esineb 2 haiguses |
| KCNJ11potassium inwardly rectifying channel subfamily J member 11 | Sageli (30–79%) | Esineb 2 haiguses |
| KCNN3potassium calcium-activated channel subfamily N member 3 | Sageli (30–79%) | Esineb 2 haiguses |
| KCNT1potassium sodium-activated channel subfamily T member 1 | Sageli (30–79%) | Esineb 1 haiguses |
| KDM2Blysine demethylase 2B | Sageli (30–79%) | Esineb 1 haiguses |
| KDM6Blysine demethylase 6B | Sageli (30–79%) | Esineb 1 haiguses |
| KIF11kinesin family member 11 | Sageli (30–79%) | Esineb 1 haiguses |
| KIF15kinesin family member 15 | Sageli (30–79%) | Esineb 1 haiguses |
| KLHL7kelch like family member 7 | Sageli (30–79%) | Esineb 1 haiguses |
| KNSTRNkinetochore localized astrin (SPAG5) binding protein | Sageli (30–79%) | Esineb 1 haiguses |
| KYNUkynureninase | Sageli (30–79%) | Esineb 1 haiguses |
| LAMA2laminin subunit alpha 2 | Sageli (30–79%) | Esineb 2 haiguses |
| LBRlamin B receptor | Sageli (30–79%) | Esineb 1 haiguses |
| LIG4DNA ligase 4 | Sageli (30–79%) | Esineb 1 haiguses |
| LMAN2Llectin, mannose binding 2 like | Sageli (30–79%) | Esineb 1 haiguses |
| LMBRD1LMBR1 domain containing 1 | Sageli (30–79%) | Esineb 1 haiguses |
| LMNB2lamin B2 | Sageli (30–79%) | Esineb 1 haiguses |
| LONP1lon peptidase 1, mitochondrial | Sageli (30–79%) | Esineb 1 haiguses |
| LRP5LDL receptor related protein 5 | Sageli (30–79%) | Esineb 1 haiguses |
| LZTR1leucine zipper like post translational regulator 1 | Sageli (30–79%) | Esineb 2 haiguses |
| MAD2L2mitotic arrest deficient 2 like 2 | Sageli (30–79%) | Esineb 1 haiguses |
| MAN2C1mannosidase alpha class 2C member 1 | Sageli (30–79%) | Esineb 1 haiguses |
| MAP1Bmicrotubule associated protein 1B | Sageli (30–79%) | Esineb 1 haiguses |
| MASP1MBL associated serine protease 1 | Sageli (30–79%) | Esineb 1 haiguses |
| MCM3APminichromosome maintenance complex component 3 associated protein | Sageli (30–79%) | Esineb 1 haiguses |
| MEG3maternally expressed 3 | Sageli (30–79%) | Esineb 3 haiguses |
| MGME1mitochondrial genome maintenance exonuclease 1 | Sageli (30–79%) | Esineb 2 haiguses |
| MICOS13mitochondrial contact site and cristae organizing system subunit 13 | Sageli (30–79%) | Esineb 1 haiguses |
| MID1midline 1 | Sageli (30–79%) | Esineb 1 haiguses |
| MLXIPLMLX interacting protein like | Sageli (30–79%) | Esineb 1 haiguses |
| MMUTmethylmalonyl-CoA mutase | Sageli (30–79%) | Esineb 2 haiguses |
| MT-TL2mitochondrially encoded tRNA-Leu (CUN) 2 | Sageli (30–79%) | Esineb 1 haiguses |
| MTFMTmitochondrial methionyl-tRNA formyltransferase | Sageli (30–79%) | Esineb 1 haiguses |
| MTO1mitochondrial tRNA translation optimization 1 | Sageli (30–79%) | Esineb 1 haiguses |
| MTRR5-methyltetrahydrofolate-homocysteine methyltransferase reductase | Sageli (30–79%) | Esineb 2 haiguses |
| MYMKmyomaker, myoblast fusion factor | Sageli (30–79%) | Esineb 1 haiguses |
| MYMXmyomixer, myoblast fusion factor | Sageli (30–79%) | Esineb 1 haiguses |
| MYSM1Myb like, SWIRM and MPN domains 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NALCNsodium leak channel, non-selective | Sageli (30–79%) | Esineb 1 haiguses |
| NDC1NDC1 transmembrane nucleoporin | Sageli (30–79%) | Esineb 1 haiguses |
| NDPnorrin cystine knot growth factor NDP | Sageli (30–79%) | Esineb 2 haiguses |
| NDUFA1NADH:ubiquinone oxidoreductase subunit A1 | Sageli (30–79%) | Esineb 1 haiguses |
| NECAP1NECAP endocytosis associated 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NECTIN1nectin cell adhesion molecule 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NEMFnuclear export mediator factor | Sageli (30–79%) | Esineb 1 haiguses |
| NEU1neuraminidase 1 | Sageli (30–79%) | Esineb 2 haiguses |
| NF1neurofibromin 1 | Sageli (30–79%) | Esineb 4 haiguses |
| NFIAnuclear factor I A | Sageli (30–79%) | Esineb 2 haiguses |
| NHP2NHP2 ribonucleoprotein | Sageli (30–79%) | Esineb 2 haiguses |
| NHSNHS actin remodeling regulator | Sageli (30–79%) | Esineb 1 haiguses |
| NIPA1NIPA magnesium transporter 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NIPA2NIPA magnesium transporter 2 | Sageli (30–79%) | Esineb 1 haiguses |
| NODALnodal growth differentiation factor | Sageli (30–79%) | Esineb 6 haiguses |
| NOTCH3notch receptor 3 | Sageli (30–79%) | Esineb 2 haiguses |
| NRCAMneuronal cell adhesion molecule | Sageli (30–79%) | Esineb 1 haiguses |
| NTRK2neurotrophic receptor tyrosine kinase 2 | Sageli (30–79%) | Esineb 2 haiguses |
| NUP54nucleoporin 54 | Sageli (30–79%) | Esineb 1 haiguses |
| OPA3outer mitochondrial membrane lipid metabolism regulator OPA3 | Sageli (30–79%) | Esineb 1 haiguses |
| PAHphenylalanine hydroxylase | Sageli (30–79%) | Esineb 2 haiguses |
| PAK2p21 (RAC1) activated kinase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| PALB2partner and localizer of BRCA2 | Sageli (30–79%) | Esineb 1 haiguses |
| PARS2prolyl-tRNA synthetase 2, mitochondrial | Sageli (30–79%) | Esineb 1 haiguses |
| PCCApropionyl-CoA carboxylase subunit alpha | Sageli (30–79%) | Esineb 1 haiguses |
| PCCBpropionyl-CoA carboxylase subunit beta | Sageli (30–79%) | Esineb 1 haiguses |
| PCDH19protocadherin 19 | Sageli (30–79%) | Esineb 2 haiguses |
| PDGFRBplatelet derived growth factor receptor beta | Sageli (30–79%) | Esineb 1 haiguses |
| PDX1pancreatic and duodenal homeobox 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PGAP1post-GPI attachment to proteins inositol deacylase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PGAP2post-GPI attachment to proteins 2 | Sageli (30–79%) | Esineb 1 haiguses |
| PGAP3post-GPI attachment to proteins phospholipase 3 | Sageli (30–79%) | Esineb 2 haiguses |
| PGK1phosphoglycerate kinase 1 | Sageli (30–79%) | Esineb 2 haiguses |
| PGM3phosphoglucomutase 3 | Sageli (30–79%) | Esineb 1 haiguses |
| PHOX2Bpaired like homeobox 2B | Sageli (30–79%) | Esineb 1 haiguses |
| PIGWphosphatidylinositol glycan anchor biosynthesis class W | Sageli (30–79%) | Esineb 2 haiguses |
| PIGYphosphatidylinositol glycan anchor biosynthesis class Y | Sageli (30–79%) | Esineb 1 haiguses |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Sageli (30–79%) | Esineb 6 haiguses |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | Sageli (30–79%) | Esineb 1 haiguses |
| PITRM1pitrilysin metallopeptidase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PLAAphospholipase A2 activating protein | Sageli (30–79%) | Esineb 1 haiguses |
| PLAAT3phospholipase A and acyltransferase 3 | Sageli (30–79%) | Esineb 1 haiguses |
| PLCH1phospholipase C eta 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PODXLpodocalyxin like | Sageli (30–79%) | Esineb 1 haiguses |
| POLR1CRNA polymerase I and III subunit C | Sageli (30–79%) | Esineb 1 haiguses |
| POLRMTRNA polymerase mitochondrial | Sageli (30–79%) | Esineb 1 haiguses |
| PORCNporcupine O-acyltransferase | Sageli (30–79%) | Esineb 2 haiguses |
| PRORPprotein only RNase P catalytic subunit | Sageli (30–79%) | Esineb 1 haiguses |
| PRPS1phosphoribosyl pyrophosphate synthetase 1 | Sageli (30–79%) | Esineb 4 haiguses |
| PRRT2proline rich transmembrane protein 2 | Sageli (30–79%) | Esineb 2 haiguses |
| PSMB8proteasome 20S subunit beta 8 | Sageli (30–79%) | Esineb 1 haiguses |
| PTBP1polypyrimidine tract binding protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PUS1pseudouridine synthase 1 | Sageli (30–79%) | Esineb 2 haiguses |
| RAD51CRAD51 paralog C | Sageli (30–79%) | Esineb 1 haiguses |
| RAF1Raf-1 proto-oncogene, serine/threonine kinase | Sageli (30–79%) | Esineb 2 haiguses |
| RANBP2RAN binding protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| RBM10RNA binding motif protein 10 | Sageli (30–79%) | Esineb 1 haiguses |
| RECQL4RecQ like helicase 4 | Sageli (30–79%) | Esineb 4 haiguses |
| RETret proto-oncogene | Sageli (30–79%) | Esineb 1 haiguses |
| RFWD3ring finger and WD repeat domain 3 | Sageli (30–79%) | Esineb 1 haiguses |
| RIPK4receptor interacting serine/threonine kinase 4 | Sageli (30–79%) | Esineb 1 haiguses |
| RMRPRNA component of mitochondrial RNA processing endoribonuclease | Sageli (30–79%) | Esineb 1 haiguses |
| RNF213ring finger protein 213 | Sageli (30–79%) | Esineb 1 haiguses |
| RNF220ring finger protein 220 | Sageli (30–79%) | Esineb 1 haiguses |
| RNU12RNA, U12 small nuclear | Sageli (30–79%) | Esineb 1 haiguses |
| RTL1retrotransposon Gag like 1 | Sageli (30–79%) | Esineb 3 haiguses |
| SCN3Asodium voltage-gated channel alpha subunit 3 | Sageli (30–79%) | Esineb 2 haiguses |
| SEMA3Esemaphorin 3E | Sageli (30–79%) | Esineb 1 haiguses |
| SEPHS1selenophosphate synthetase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SETBP1SET binding protein 1 | Sageli (30–79%) | Esineb 2 haiguses |
| SH2B1SH2B adaptor protein 1 | Sageli (30–79%) | Esineb 2 haiguses |
| SHANK3SH3 and multiple ankyrin repeat domains 3 | Sageli (30–79%) | Esineb 1 haiguses |
| SHHsonic hedgehog signaling molecule | Sageli (30–79%) | Esineb 7 haiguses |
| SIM1SIM bHLH transcription factor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SIN3ASIN3 transcription regulator family member A | Sageli (30–79%) | Esineb 2 haiguses |
| SIX3SIX homeobox 3 | Sageli (30–79%) | Esineb 7 haiguses |
| SLC13A5solute carrier family 13 member 5 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC16A1solute carrier family 16 member 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC1A2solute carrier family 1 member 2 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC1A3solute carrier family 1 member 3 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC25A15solute carrier family 25 member 15 | Sageli (30–79%) | Esineb 2 haiguses |
| SLC35A3solute carrier family 35 member A3 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC39A14solute carrier family 39 member 14 | Sageli (30–79%) | Esineb 2 haiguses |
| SLC5A7solute carrier family 5 member 7 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC7A7solute carrier family 7 member 7 | Sageli (30–79%) | Esineb 2 haiguses |
| SLX4SLX4 structure-specific endonuclease subunit | Sageli (30–79%) | Esineb 1 haiguses |
| SMOsmoothened, frizzled class receptor | Sageli (30–79%) | Esineb 1 haiguses |
| SNRPBsmall nuclear ribonucleoprotein polypeptides B and B1 | Sageli (30–79%) | Esineb 2 haiguses |
| SPG11SPG11 vesicle trafficking associated, spatacsin | Sageli (30–79%) | Esineb 2 haiguses |
| SPRsepiapterin reductase | Sageli (30–79%) | Esineb 2 haiguses |
| SPTAN1spectrin alpha, non-erythrocytic 1 | Sageli (30–79%) | Esineb 2 haiguses |
| SRCAPSnf2 related CREBBP activator protein | Sageli (30–79%) | Esineb 2 haiguses |
| SRPX2sushi repeat containing protein X-linked 2 | Sageli (30–79%) | Esineb 2 haiguses |
| STAG2STAG2 cohesin complex component | Sageli (30–79%) | Esineb 3 haiguses |
| STAT3signal transducer and activator of transcription 3 | Sageli (30–79%) | Esineb 1 haiguses |
| STSsteroid sulfatase | Sageli (30–79%) | Esineb 3 haiguses |
| STXBP1syntaxin binding protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SUCLG1succinate-CoA ligase GDP/ADP-forming subunit alpha | Sageli (30–79%) | Esineb 1 haiguses |
| SYNJ1synaptojanin 1 | Sageli (30–79%) | Esineb 2 haiguses |
| SYT1synaptotagmin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SZT2SZT2 subunit of KICSTOR complex | Sageli (30–79%) | Esineb 1 haiguses |
| TAOK1TAO kinase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TBCBtubulin folding cofactor B | Sageli (30–79%) | Esineb 1 haiguses |
| TCP1t-complex 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TGIF1TGFB induced factor homeobox 1 | Sageli (30–79%) | Esineb 6 haiguses |
| TKTtransketolase | Sageli (30–79%) | Esineb 1 haiguses |
| TMEM240transmembrane protein 240 | Sageli (30–79%) | Esineb 2 haiguses |
| TONSLtonsoku like, DNA repair protein | Sageli (30–79%) | Esineb 1 haiguses |
| TOPORSTOP1 binding arginine/serine rich protein, E3 ubiquitin ligase | Sageli (30–79%) | Esineb 1 haiguses |
| TRAF7TNF receptor associated factor 7 | Sageli (30–79%) | Esineb 1 haiguses |
| TRAK1trafficking kinesin protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TRAPPC11trafficking protein particle complex subunit 11 | Sageli (30–79%) | Esineb 3 haiguses |
| TRIP13thyroid hormone receptor interactor 13 | Sageli (30–79%) | Esineb 1 haiguses |
| TRPS1transcriptional repressor GATA binding 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TSC1TSC complex subunit 1 | Sageli (30–79%) | Esineb 3 haiguses |
| TSC2TSC complex subunit 2 | Sageli (30–79%) | Esineb 3 haiguses |
| TUBG1tubulin gamma 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TUBGCP4tubulin gamma complex component 4 | Sageli (30–79%) | Esineb 1 haiguses |
| TUBGCP6tubulin gamma complex component 6 | Sageli (30–79%) | Esineb 2 haiguses |
| UBA5ubiquitin like modifier activating enzyme 5 | Sageli (30–79%) | Esineb 1 haiguses |
| UBE2Tubiquitin conjugating enzyme E2 T | Sageli (30–79%) | Esineb 1 haiguses |
| UBR1ubiquitin protein ligase E3 component n-recognin 1 | Sageli (30–79%) | Esineb 2 haiguses |
| UBR5ubiquitin protein ligase E3 component n-recognin 5 | Sageli (30–79%) | Esineb 1 haiguses |
| UHRF1ubiquitin like with PHD and ring finger domains 1 | Sageli (30–79%) | Esineb 1 haiguses |
| UPB1beta-ureidopropionase 1 | Sageli (30–79%) | Esineb 2 haiguses |
| VIPAS39VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog | Sageli (30–79%) | Esineb 1 haiguses |
| VPS33BVPS33B late endosome and lysosome associated | Sageli (30–79%) | Esineb 1 haiguses |
| WDR45WD repeat domain 45 | Sageli (30–79%) | Esineb 2 haiguses |
| WT1WT1 transcription factor | Sageli (30–79%) | Esineb 2 haiguses |
| XPNPEP3X-prolyl aminopeptidase 3 | Sageli (30–79%) | Esineb 1 haiguses |
| XRCC2X-ray repair cross complementing 2 | Sageli (30–79%) | Esineb 1 haiguses |
| YARS2tyrosyl-tRNA synthetase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| ZFYVE26zinc finger FYVE-type containing 26 | Sageli (30–79%) | Esineb 2 haiguses |
| ZIC2Zic family zinc finger 2 | Sageli (30–79%) | Esineb 7 haiguses |
| ZNF699zinc finger protein 699 | Sageli (30–79%) | Esineb 1 haiguses |
| AAASaladin WD repeat nucleoporin | Mõnikord (5–29%) | Esineb 2 haiguses |
| ACP5acid phosphatase 5, tartrate resistant | Mõnikord (5–29%) | Esineb 1 haiguses |
| ADRA2Badrenoceptor alpha 2B | Mõnikord (5–29%) | Esineb 1 haiguses |
| AGGF1angiogenic factor with G-patch and FHA domains 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| AIPL1AIP like 1 HSP90 co-chaperone | Mõnikord (5–29%) | Esineb 1 haiguses |
| AKT1AKT serine/threonine kinase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ALDH7A1aldehyde dehydrogenase 7 family member A1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| ALDOAaldolase, fructose-bisphosphate A | Mõnikord (5–29%) | Esineb 2 haiguses |
| ALMS1ALMS1 centrosome and basal body associated protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| ALX4ALX homeobox 4 | Mõnikord (5–29%) | Esineb 3 haiguses |
| AMER1APC membrane recruitment protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ANAPC1anaphase promoting complex subunit 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ANO10anoctamin 10 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ARHGAP31Rho GTPase activating protein 31 | Mõnikord (5–29%) | Esineb 2 haiguses |
| ARNT2aryl hydrocarbon receptor nuclear translocator 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ARVCFARVCF delta catenin family member | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATAD1ATPase family AAA domain containing 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATP2A2ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| BBS10Bardet-Biedl syndrome 10 | Mõnikord (5–29%) | Esineb 1 haiguses |
| BBS12Bardet-Biedl syndrome 12 | Mõnikord (5–29%) | Esineb 1 haiguses |
| BBS5Bardet-Biedl syndrome 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| BCS1LBCS1 ubiquinol-cytochrome c reductase complex chaperone | Mõnikord (5–29%) | Esineb 3 haiguses |
| BICD2BICD cargo adaptor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| BTDbiotinidase | Mõnikord (5–29%) | Esineb 1 haiguses |
| CABP4calcium binding protein 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CACNA1Ccalcium voltage-gated channel subunit alpha1 C | Mõnikord (5–29%) | Esineb 2 haiguses |
| CACNA1Hcalcium voltage-gated channel subunit alpha1 H | Mõnikord (5–29%) | Esineb 1 haiguses |
| CBLCbl proto-oncogene | Mõnikord (5–29%) | Esineb 1 haiguses |
| CCDC78coiled-coil domain containing 78 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CDC45cell division cycle 45 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CDC6cell division cycle 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CDT1chromatin licensing and DNA replication factor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CEP19centrosomal protein 19 | Mõnikord (5–29%) | Esineb 2 haiguses |
| CFAP418cilia and flagella associated protein 418 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CHD6chromodomain helicase DNA binding protein 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CHRNA4cholinergic receptor nicotinic alpha 4 subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| CHST14carbohydrate sulfotransferase 14 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CISD2CDGSH iron sulfur domain 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CLTRNcollectrin, amino acid transport regulator | Mõnikord (5–29%) | Esineb 1 haiguses |
| CNTN2contactin 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| COL13A1collagen type XIII alpha 1 chain | Mõnikord (5–29%) | Esineb 1 haiguses |
| COL25A1collagen type XXV alpha 1 chain | Mõnikord (5–29%) | Esineb 1 haiguses |
| COL2A1collagen type II alpha 1 chain | Mõnikord (5–29%) | Esineb 2 haiguses |
| COLQcollagen like tail subunit of asymmetric acetylcholinesterase | Mõnikord (5–29%) | Esineb 1 haiguses |
| COMTcatechol-O-methyltransferase | Mõnikord (5–29%) | Esineb 1 haiguses |
| COQ8Acoenzyme Q8A | Mõnikord (5–29%) | Esineb 1 haiguses |
| CPA6carboxypeptidase A6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CRB1crumbs cell polarity complex component 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CRLF1cytokine receptor like factor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CRXcone-rod homeobox | Mõnikord (5–29%) | Esineb 1 haiguses |
| CSF1Rcolony stimulating factor 1 receptor | Mõnikord (5–29%) | Esineb 1 haiguses |
| CSTBcystatin B | Mõnikord (5–29%) | Esineb 1 haiguses |
| CTNND2catenin delta 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CYP2U1cytochrome P450 family 2 subfamily U member 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| DACT1dishevelled binding antagonist of beta catenin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DHTKD1dehydrogenase E1 and transketolase domain containing 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DIP2BDIP2 acetate--CoA ligase B (putative) | Mõnikord (5–29%) | Esineb 1 haiguses |
| DLL3delta like canonical Notch ligand 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DLL4delta like canonical Notch ligand 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DNAJB4DnaJ heat shock protein family (Hsp40) member B4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DNAJC21DnaJ heat shock protein family (Hsp40) member C21 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DOCK6dedicator of cytokinesis 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DOLKdolichol kinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| DONSONDNA replication fork stabilization factor DONSON | Mõnikord (5–29%) | Esineb 1 haiguses |
| DSG4desmoglein 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DSTdystonin | Mõnikord (5–29%) | Esineb 1 haiguses |
| DUOX2dual oxidase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DUOXA2dual oxidase maturation factor 2 | Mõnikord (5–29%) | Esineb 2 haiguses |
| DVL1dishevelled segment polarity protein 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| DVL3dishevelled segment polarity protein 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DYNC2LI1dynein cytoplasmic 2 light intermediate chain 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| EFL1elongation factor like GTPase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| EIF2AK2eukaryotic translation initiation factor 2 alpha kinase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| EIF2AK3eukaryotic translation initiation factor 2 alpha kinase 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| EOGTEGF domain specific O-linked N-acetylglucosamine transferase | Mõnikord (5–29%) | Esineb 1 haiguses |
| EVCEvC ciliary complex subunit 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| EVC2EvC ciliary complex subunit 2 | Mõnikord (5–29%) | Esineb 2 haiguses |
| EXT2exostosin glycosyltransferase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FBP1fructose-bisphosphatase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FLNBfilamin B | Mõnikord (5–29%) | Esineb 2 haiguses |
| FOXI1forkhead box I1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| FOXP2forkhead box P2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FRAS1Fraser extracellular matrix complex subunit 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| FREM2FRAS1 related extracellular matrix 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FZD2frizzled class receptor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GAAalpha glucosidase | Mõnikord (5–29%) | Esineb 1 haiguses |
| GALK1galactokinase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GBA1glucosylceramidase beta 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GBA2glucosylceramidase beta 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GCLCglutamate-cysteine ligase catalytic subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| GDF6growth differentiation factor 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GHRgrowth hormone receptor | Mõnikord (5–29%) | Esineb 1 haiguses |
| GJA1gap junction protein alpha 1 | Mõnikord (5–29%) | Esineb 3 haiguses |
| GJB3gap junction protein beta 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GJB4gap junction protein beta 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GLI1GLI family zinc finger 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GLI3GLI family zinc finger 3 | Mõnikord (5–29%) | Esineb 2 haiguses |
| GLRA1glycine receptor alpha 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GLRBglycine receptor beta | Mõnikord (5–29%) | Esineb 2 haiguses |
| GMNNgeminin DNA replication inhibitor | Mõnikord (5–29%) | Esineb 2 haiguses |
| GP1BBglycoprotein Ib platelet subunit beta | Mõnikord (5–29%) | Esineb 1 haiguses |
| GPC3glypican 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GPC6glypican 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GPHNgephyrin | Mõnikord (5–29%) | Esineb 1 haiguses |
| GPIglucose-6-phosphate isomerase | Mõnikord (5–29%) | Esineb 2 haiguses |
| GPR161G protein-coupled receptor 161 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GPRC5BG protein-coupled receptor class C group 5 member B | Mõnikord (5–29%) | Esineb 1 haiguses |
| GRIP1glutamate receptor interacting protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GUCY2Dguanylate cyclase 2D, retinal | Mõnikord (5–29%) | Esineb 2 haiguses |
| H19H19 imprinted maternally expressed transcript | Mõnikord (5–29%) | Esineb 1 haiguses |
| HADHAhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | Mõnikord (5–29%) | Esineb 1 haiguses |
| HCCSholocytochrome c synthase | Mõnikord (5–29%) | Esineb 2 haiguses |
| HDAC6histone deacetylase 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HES7hes family bHLH transcription factor 7 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HESX1HESX homeobox 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| HIRAhistone cell cycle regulator | Mõnikord (5–29%) | Esineb 1 haiguses |
| HNF1BHNF1 homeobox B | Mõnikord (5–29%) | Esineb 2 haiguses |
| HNRNPA1heterogeneous nuclear ribonucleoprotein A1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HNRNPA2B1heterogeneous nuclear ribonucleoprotein A2/B1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IFT172intraflagellar transport 172 | Mõnikord (5–29%) | Esineb 2 haiguses |
| IFT27intraflagellar transport 27 | Mõnikord (5–29%) | Esineb 2 haiguses |
| IGF2insulin like growth factor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | Mõnikord (5–29%) | Esineb 2 haiguses |
| IMPDH1inosine monophosphate dehydrogenase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IQCB1IQ motif containing B1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ITPR3inositol 1,4,5-trisphosphate receptor type 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IYDiodotyrosine deiodinase | Mõnikord (5–29%) | Esineb 2 haiguses |
| JMJD1Cjumonji domain containing 1C | Mõnikord (5–29%) | Esineb 1 haiguses |
| JRKJrk helix-turn-helix protein | Mõnikord (5–29%) | Esineb 2 haiguses |
| KCNJ13potassium inwardly rectifying channel subfamily J member 13 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KDSR3-ketodihydrosphingosine reductase | Mõnikord (5–29%) | Esineb 1 haiguses |
| KIF21Akinesin family member 21A | Mõnikord (5–29%) | Esineb 1 haiguses |
| KITKIT proto-oncogene, receptor tyrosine kinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| KRT81keratin 81 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KRT83keratin 83 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KRT86keratin 86 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KYkyphoscoliosis peptidase | Mõnikord (5–29%) | Esineb 1 haiguses |
| LAMB2laminin subunit beta 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LCA5lebercilin LCA5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LFNGLFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase | Mõnikord (5–29%) | Esineb 1 haiguses |
| LHX1LIM homeobox 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LHX4LIM homeobox 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LIG3DNA ligase 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LMBR1limb development membrane protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LMNAlamin A/C | Mõnikord (5–29%) | Esineb 3 haiguses |
| LRATlecithin retinol acyltransferase | Mõnikord (5–29%) | Esineb 1 haiguses |
| LRRK1leucine rich repeat kinase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAP3K7mitogen-activated protein kinase kinase kinase 7 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MARCHF6membrane associated ring-CH-type finger 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAT1Amethionine adenosyltransferase 1A | Mõnikord (5–29%) | Esineb 1 haiguses |
| MCCC2methylcrotonyl-CoA carboxylase subunit 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MESP2mesoderm posterior bHLH transcription factor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MLC1modulator of VRAC current 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MMP14matrix metallopeptidase 14 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MMP2matrix metallopeptidase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MRASmuscle RAS oncogene homolog | Mõnikord (5–29%) | Esineb 1 haiguses |
| MTHFRmethylenetetrahydrofolate reductase | Mõnikord (5–29%) | Esineb 1 haiguses |
| MTRFRmitochondrial translation release factor in rescue | Mõnikord (5–29%) | Esineb 1 haiguses |
| NDUFB11NADH:ubiquinone oxidoreductase subunit B11 | Mõnikord (5–29%) | Esineb 2 haiguses |
| NLRP3NLR family pyrin domain containing 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NMNAT1nicotinamide nucleotide adenylyltransferase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NOTCH1notch receptor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NPRL2NPR2 like, GATOR1 complex subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| NPRL3NPR3 like, GATOR1 complex subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| NXNnucleoredoxin | Mõnikord (5–29%) | Esineb 1 haiguses |
| ORC1origin recognition complex subunit 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ORC4origin recognition complex subunit 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ORC6origin recognition complex subunit 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| OTX2orthodenticle homeobox 2 | Mõnikord (5–29%) | Esineb 2 haiguses |
| PAX3paired box 3 | Mõnikord (5–29%) | Esineb 2 haiguses |
| PCYT1Aphosphate cytidylyltransferase 1A, choline | Mõnikord (5–29%) | Esineb 2 haiguses |
| PEPDpeptidase D | Mõnikord (5–29%) | Esineb 1 haiguses |
| PEX16peroxisomal biogenesis factor 16 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PHKA2phosphorylase kinase regulatory subunit alpha 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PHKG2phosphorylase kinase catalytic subunit gamma 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PHOX2Apaired like homeobox 2A | Mõnikord (5–29%) | Esineb 1 haiguses |
| PLPBPpyridoxal phosphate binding protein | Mõnikord (5–29%) | Esineb 2 haiguses |
| PMM2phosphomannomutase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PNPpurine nucleoside phosphorylase | Mõnikord (5–29%) | Esineb 2 haiguses |
| PNPLA2patatin like domain 2, triacylglycerol lipase | Mõnikord (5–29%) | Esineb 1 haiguses |
| POLGDNA polymerase gamma, catalytic subunit | Mõnikord (5–29%) | Esineb 2 haiguses |
| PPP1CBprotein phosphatase 1 catalytic subunit beta | Mõnikord (5–29%) | Esineb 1 haiguses |
| PPP1R13Lprotein phosphatase 1 regulatory subunit 13 like | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRDM12PR/SET domain 12 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRICKLE1prickle planar cell polarity protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRKACAprotein kinase cAMP-activated catalytic subunit alpha | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRKACBprotein kinase cAMP-activated catalytic subunit beta | Mõnikord (5–29%) | Esineb 1 haiguses |
| PROKR2prokineticin receptor 2 | Mõnikord (5–29%) | Esineb 2 haiguses |
| PRPH2peripherin 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PSEN1presenilin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PSEN2presenilin 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PTCH2patched 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PTPN11protein tyrosine phosphatase non-receptor type 11 | Mõnikord (5–29%) | Esineb 2 haiguses |
| PTS6-pyruvoyltetrahydropterin synthase | Mõnikord (5–29%) | Esineb 2 haiguses |
| RAPGEF2Rap guanine nucleotide exchange factor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RASA2RAS p21 protein activator 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RBPJrecombination signal binding protein for immunoglobulin kappa J region | Mõnikord (5–29%) | Esineb 1 haiguses |
| RD3RD3 regulator of GUCY2D | Mõnikord (5–29%) | Esineb 1 haiguses |
| RDH12retinol dehydrogenase 12 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RIPPLY2ripply transcriptional repressor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RIT1Ras like without CAAX 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| ROR2ROR family WNT receptor 2 | Mõnikord (5–29%) | Esineb 2 haiguses |
| RPE65retinoid isomerohydrolase RPE65 | Mõnikord (5–29%) | Esineb 2 haiguses |
| RPGRIP1RPGR interacting protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RRASRAS related | Mõnikord (5–29%) | Esineb 1 haiguses |
| RRAS2RAS related 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RREB1ras responsive element binding protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Mõnikord (5–29%) | Esineb 2 haiguses |
| SALL1spalt like transcription factor 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| SAMD12sterile alpha motif domain containing 12 | Mõnikord (5–29%) | Esineb 2 haiguses |
| SBDSSBDS ribosome maturation factor | Mõnikord (5–29%) | Esineb 1 haiguses |
| SCARB2scavenger receptor class B member 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SCLT1sodium channel and clathrin linker 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SCUBE3signal peptide, CUB domain and EGF like domain containing 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SEC24CSEC24 homolog C, COPII component | Mõnikord (5–29%) | Esineb 1 haiguses |
| SECISBP2SECIS binding protein 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SF3B4splicing factor 3b subunit 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC1A1solute carrier family 1 member 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| SLC26A4solute carrier family 26 member 4 | Mõnikord (5–29%) | Esineb 2 haiguses |
| SLC2A10solute carrier family 2 member 10 | Mõnikord (5–29%) | Esineb 2 haiguses |
| SLC5A5solute carrier family 5 member 5 | Mõnikord (5–29%) | Esineb 2 haiguses |
| SLC6A5solute carrier family 6 member 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SMCHD1structural maintenance of chromosomes flexible hinge domain containing 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SMPD1sphingomyelin phosphodiesterase 1 | Mõnikord (5–29%) | Esineb 3 haiguses |
| SNAI2snail family transcriptional repressor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SORL1sortilin related receptor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SOS1SOS Ras/Rac guanine nucleotide exchange factor 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| SOS2SOS Ras/Rho guanine nucleotide exchange factor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SOX2SRY-box transcription factor 2 | Mõnikord (5–29%) | Esineb 2 haiguses |
| SPATA7spermatogenesis associated 7 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SPINK5serine peptidase inhibitor Kazal type 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SPRED2sprouty related EVH1 domain containing 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| STAC3SH3 and cysteine rich domain 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SYNE1spectrin repeat containing nuclear envelope protein 1 | Mõnikord (5–29%) | Esineb 3 haiguses |
| TBX6T-box transcription factor 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TCF12transcription factor 12 | Mõnikord (5–29%) | Esineb 2 haiguses |
| TGthyroglobulin | Mõnikord (5–29%) | Esineb 2 haiguses |
| TGFBR2transforming growth factor beta receptor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TMEM106Btransmembrane protein 106B | Mõnikord (5–29%) | Esineb 1 haiguses |
| TNRC6Atrinucleotide repeat containing adaptor 6A | Mõnikord (5–29%) | Esineb 1 haiguses |
| TOMM40translocase of outer mitochondrial membrane 40 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TP53RKTP53 regulating kinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| TP63tumor protein p63 | Mõnikord (5–29%) | Esineb 2 haiguses |
| TPOthyroid peroxidase | Mõnikord (5–29%) | Esineb 1 haiguses |
| TREM2triggering receptor expressed on myeloid cells 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TRIM32tripartite motif containing 32 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TTC8tetratricopeptide repeat domain 8 | Mõnikord (5–29%) | Esineb 2 haiguses |
| TUBA1Atubulin alpha 1a | Mõnikord (5–29%) | Esineb 1 haiguses |
| TUBB4Btubulin beta 4B class IVb | Mõnikord (5–29%) | Esineb 1 haiguses |
| TULP1TUB like protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TWIST1twist family bHLH transcription factor 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| TWIST2twist family bHLH transcription factor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TYMPthymidine phosphorylase | Mõnikord (5–29%) | Esineb 2 haiguses |
| UFD1ubiquitin recognition factor in ER associated degradation 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| UGT1A1UDP glucuronosyltransferase family 1 member A1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| USP45ubiquitin specific peptidase 45 | Mõnikord (5–29%) | Esineb 1 haiguses |
| USP8ubiquitin specific peptidase 8 | Mõnikord (5–29%) | Esineb 1 haiguses |
| VCPvalosin containing protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| WDPCPWD repeat containing planar cell polarity effector | Mõnikord (5–29%) | Esineb 1 haiguses |
| WDR11WD repeat domain 11 | Mõnikord (5–29%) | Esineb 1 haiguses |
| WFS1wolframin ER transmembrane glycoprotein | Mõnikord (5–29%) | Esineb 2 haiguses |
| WNT5AWnt family member 5A | Mõnikord (5–29%) | Esineb 2 haiguses |
| XYLT2xylosyltransferase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| YEATS2YEATS domain containing 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ZIC4Zic family zinc finger 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ZMYM2zinc finger MYM-type containing 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ACVR1activin A receptor type 1 | Harva (1–4%) | Esineb 1 haiguses |
| ANTXR1ANTXR cell adhesion molecule 1 | Harva (1–4%) | Esineb 1 haiguses |
| DARS2aspartyl-tRNA synthetase 2, mitochondrial | Harva (1–4%) | Esineb 1 haiguses |
| FLGfilaggrin | Harva (1–4%) | Esineb 1 haiguses |
| MC2Rmelanocortin 2 receptor | Harva (1–4%) | Esineb 1 haiguses |
| MRAPmelanocortin 2 receptor accessory protein | Harva (1–4%) | Esineb 1 haiguses |
| MSX2msh homeobox 2 | Harva (1–4%) | Esineb 1 haiguses |
| MYRFmyelin regulatory factor | Harva (1–4%) | Esineb 1 haiguses |
| NKX6-2NK6 homeobox 2 | Harva (1–4%) | Esineb 1 haiguses |
| NNTnicotinamide nucleotide transhydrogenase | Harva (1–4%) | Esineb 1 haiguses |
| PRKRAprotein activator of interferon induced protein kinase EIF2AK2 | Harva (1–4%) | Esineb 1 haiguses |
| RBM8ARNA binding motif protein 8A | Harva (1–4%) | Esineb 1 haiguses |
| RPS19ribosomal protein S19 | Harva (1–4%) | Esineb 1 haiguses |
| SPASTspastin | Harva (1–4%) | Esineb 2 haiguses |
| STARsteroidogenic acute regulatory protein | Harva (1–4%) | Esineb 1 haiguses |
| STARD7StAR related lipid transfer domain containing 7 | Harva (1–4%) | Esineb 1 haiguses |
| TCOF1treacle ribosome biogenesis factor 1 | Harva (1–4%) | Esineb 1 haiguses |
| TLR3toll like receptor 3 | Harva (1–4%) | Esineb 1 haiguses |
| TXNRD2thioredoxin reductase 2 | Harva (1–4%) | Esineb 1 haiguses |
| ABCA2ATP binding cassette subfamily A member 2 | Pole registreeritud | Esineb 1 haiguses |
| ABHD5abhydrolase domain containing 5, lysophosphatidic acid acyltransferase | Pole registreeritud | Esineb 1 haiguses |
| ACAT1acetyl-CoA acetyltransferase 1 | Pole registreeritud | Esineb 1 haiguses |
| ACOX1acyl-CoA oxidase 1 | Pole registreeritud | Esineb 1 haiguses |
| ADCY5adenylate cyclase 5 | Pole registreeritud | Esineb 1 haiguses |
| AFG2BAAA ATPase AFG2B | Pole registreeritud | Esineb 1 haiguses |
| AHCYadenosylhomocysteinase | Pole registreeritud | Esineb 1 haiguses |
| AKT3AKT serine/threonine kinase 3 | Pole registreeritud | Esineb 1 haiguses |
| ALDOBaldolase, fructose-bisphosphate B | Pole registreeritud | Esineb 1 haiguses |
| ALX3ALX homeobox 3 | Pole registreeritud | Esineb 1 haiguses |
| AMMECR1AMMECR nuclear protein 1 | Pole registreeritud | Esineb 1 haiguses |
| AP4M1adaptor related protein complex 4 subunit mu 1 | Pole registreeritud | Esineb 1 haiguses |
| APTXaprataxin | Pole registreeritud | Esineb 1 haiguses |
| AQP2aquaporin 2 | Pole registreeritud | Esineb 1 haiguses |
| ARCN1archain 1 coat protein complex I subunit delta | Pole registreeritud | Esineb 1 haiguses |
| ARFGEF2ARF guanine nucleotide exchange factor 2 | Pole registreeritud | Esineb 1 haiguses |
| ARG1arginase 1 | Pole registreeritud | Esineb 1 haiguses |
| ARHGDIARho GDP dissociation inhibitor alpha | Pole registreeritud | Esineb 1 haiguses |
| ARID1BAT-rich interaction domain 1B | Pole registreeritud | Esineb 1 haiguses |
| ARSAarylsulfatase A | Pole registreeritud | Esineb 1 haiguses |
| ASS1argininosuccinate synthase 1 | Pole registreeritud | Esineb 1 haiguses |
| ASXL2ASXL transcriptional regulator 2 | Pole registreeritud | Esineb 1 haiguses |
| ATP2B3ATPase plasma membrane Ca2+ transporting 3 | Pole registreeritud | Esineb 1 haiguses |
| ATP5F1EATP synthase F1 subunit epsilon | Pole registreeritud | Esineb 1 haiguses |
| AVPR2arginine vasopressin receptor 2 | Pole registreeritud | Esineb 1 haiguses |
| BAP1BRCA1 associated deubiquitinase 1 | Pole registreeritud | Esineb 1 haiguses |
| BCKDHAbranched chain keto acid dehydrogenase E1 subunit alpha | Pole registreeritud | Esineb 1 haiguses |
| BLTP1bridge-like lipid transfer protein family member 1 | Pole registreeritud | Esineb 1 haiguses |
| BPTFbromodomain PHD finger transcription factor | Pole registreeritud | Esineb 1 haiguses |
| BRAT1BRCA1 associated ATM activator 1 | Pole registreeritud | Esineb 1 haiguses |
| BSNDbarttin CLCNK type accessory subunit beta | Pole registreeritud | Esineb 1 haiguses |
| CACNB4calcium voltage-gated channel auxiliary subunit beta 4 | Pole registreeritud | Esineb 1 haiguses |
| CAMK2Bcalcium/calmodulin dependent protein kinase II beta | Pole registreeritud | Esineb 1 haiguses |
| CCDC88Ccoiled-coil and HOOK domain protein 88C | Pole registreeritud | Esineb 1 haiguses |
| CERS1ceramide synthase 1 | Pole registreeritud | Esineb 1 haiguses |
| CHMP1Acharged multivesicular body protein 1A | Pole registreeritud | Esineb 1 haiguses |
| CICcapicua transcriptional repressor | Pole registreeritud | Esineb 1 haiguses |
| CILK1ciliogenesis associated kinase 1 | Pole registreeritud | Esineb 1 haiguses |
| CLCN2chloride voltage-gated channel 2 | Pole registreeritud | Esineb 1 haiguses |
| CLCNKAchloride voltage-gated channel Ka | Pole registreeritud | Esineb 1 haiguses |
| CLCNKBchloride voltage-gated channel Kb | Pole registreeritud | Esineb 1 haiguses |
| CLN3CLN3 lysosomal/endosomal transmembrane protein, battenin | Pole registreeritud | Esineb 1 haiguses |
| CLN5CLN5 lysosomal BMP synthase | Pole registreeritud | Esineb 1 haiguses |
| CNOT3CCR4-NOT transcription complex subunit 3 | Pole registreeritud | Esineb 1 haiguses |
| COQ2coenzyme Q2, polyprenyltransferase | Pole registreeritud | Esineb 1 haiguses |
| COX10cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10 | Pole registreeritud | Esineb 1 haiguses |
| COX15cytochrome c oxidase assembly factor COX15 | Pole registreeritud | Esineb 1 haiguses |
| COX6B1cytochrome c oxidase subunit 6B1 | Pole registreeritud | Esineb 1 haiguses |
| CPS1carbamoyl-phosphate synthase 1 | Pole registreeritud | Esineb 1 haiguses |
| CTDP1CTD phosphatase 1 | Pole registreeritud | Esineb 1 haiguses |
| CTSDcathepsin D | Pole registreeritud | Esineb 1 haiguses |
| CYB5R3cytochrome b5 reductase 3 | Pole registreeritud | Esineb 1 haiguses |
| D2HGDHD-2-hydroxyglutarate dehydrogenase | Pole registreeritud | Esineb 1 haiguses |
| DCHS1dachsous cadherin-related 1 | Pole registreeritud | Esineb 1 haiguses |
| DCXdoublecortin | Pole registreeritud | Esineb 1 haiguses |
| DDX11DEAD/H-box helicase 11 | Pole registreeritud | Esineb 1 haiguses |
| DHX16DEAH-box helicase 16 | Pole registreeritud | Esineb 1 haiguses |
| DMPKDM1 protein kinase | Pole registreeritud | Esineb 1 haiguses |
| DOHHdeoxyhypusine hydroxylase | Pole registreeritud | Esineb 1 haiguses |
| DPAGT1dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 | Pole registreeritud | Esineb 1 haiguses |
| EDEM3ER degradation enhancing alpha-mannosidase like protein 3 | Pole registreeritud | Esineb 1 haiguses |
| EFHC1EF-hand domain containing 1 | Pole registreeritud | Esineb 1 haiguses |
| EIF2S3eukaryotic translation initiation factor 2 subunit gamma | Pole registreeritud | Esineb 1 haiguses |
| EMC1ER membrane protein complex subunit 1 | Pole registreeritud | Esineb 1 haiguses |
| EMDemerin | Pole registreeritud | Esineb 1 haiguses |
| ENTPD1ectonucleoside triphosphate diphosphohydrolase 1 | Pole registreeritud | Esineb 1 haiguses |
| FAM50Afamily with sequence similarity 50 member A | Pole registreeritud | Esineb 1 haiguses |
| FASTKD2FASTK mitochondrial RNA regulator 2 | Pole registreeritud | Esineb 1 haiguses |
| FHL1four and a half LIM domains 1 | Pole registreeritud | Esineb 1 haiguses |
| FOLR1folate receptor alpha | Pole registreeritud | Esineb 1 haiguses |
| FRG1FSHD region gene 1 | Pole registreeritud | Esineb 1 haiguses |
| FRMD4AFERM domain containing 4A | Pole registreeritud | Esineb 1 haiguses |
| FTCDformimidoyltransferase cyclodeaminase | Pole registreeritud | Esineb 1 haiguses |
| GALTgalactose-1-phosphate uridylyltransferase | Pole registreeritud | Esineb 1 haiguses |
| GAMTguanidinoacetate N-methyltransferase | Pole registreeritud | Esineb 1 haiguses |
| GCH1GTP cyclohydrolase 1 | Pole registreeritud | Esineb 2 haiguses |
| GJA5gap junction protein alpha 5 | Pole registreeritud | Esineb 1 haiguses |
| GJA8gap junction protein alpha 8 | Pole registreeritud | Esineb 1 haiguses |
| GLDCglycine decarboxylase | Pole registreeritud | Esineb 1 haiguses |
| GLUD1glutamate dehydrogenase 1 | Pole registreeritud | Esineb 1 haiguses |
| GNPATglyceronephosphate O-acyltransferase | Pole registreeritud | Esineb 1 haiguses |
| GNSglucosamine (N-acetyl)-6-sulfatase | Pole registreeritud | Esineb 1 haiguses |
| GPAA1glycosylphosphatidylinositol anchor attachment 1 | Pole registreeritud | Esineb 1 haiguses |
| GPR88G protein-coupled receptor 88 | Pole registreeritud | Esineb 1 haiguses |
| HADHhydroxyacyl-CoA dehydrogenase | Pole registreeritud | Esineb 1 haiguses |
| HCFC1host cell factor C1 | Pole registreeritud | Esineb 1 haiguses |
| HNMThistamine N-methyltransferase | Pole registreeritud | Esineb 1 haiguses |
| HNRNPKheterogeneous nuclear ribonucleoprotein K | Pole registreeritud | Esineb 1 haiguses |
| IFIH1interferon induced with helicase C domain 1 | Pole registreeritud | Esineb 1 haiguses |
| IMPDH2inosine monophosphate dehydrogenase 2 | Pole registreeritud | Esineb 1 haiguses |
| INPP5Kinositol polyphosphate-5-phosphatase K | Pole registreeritud | Esineb 1 haiguses |
| KANK1KN motif and ankyrin repeat domains 1 | Pole registreeritud | Esineb 1 haiguses |
| KANSL1KAT8 regulatory NSL complex subunit 1 | Pole registreeritud | Esineb 1 haiguses |
| KCNC3potassium voltage-gated channel subfamily C member 3 | Pole registreeritud | Esineb 1 haiguses |
| KCNJ1potassium inwardly rectifying channel subfamily J member 1 | Pole registreeritud | Esineb 1 haiguses |
| KCNK9potassium two pore domain channel subfamily K member 9 | Pole registreeritud | Esineb 1 haiguses |
| KCNQ3potassium voltage-gated channel subfamily Q member 3 | Pole registreeritud | Esineb 1 haiguses |
| KDM3Blysine demethylase 3B | Pole registreeritud | Esineb 1 haiguses |
| KIF14kinesin family member 14 | Pole registreeritud | Esineb 1 haiguses |
| LDHDlactate dehydrogenase D | Pole registreeritud | Esineb 1 haiguses |
| LHX3LIM homeobox 3 | Pole registreeritud | Esineb 1 haiguses |
| MADDMAP kinase activating death domain | Pole registreeritud | Esineb 1 haiguses |
| MAOAmonoamine oxidase A | Pole registreeritud | Esineb 1 haiguses |
| MCCC1methylcrotonyl-CoA carboxylase subunit 1 | Pole registreeritud | Esineb 1 haiguses |
| MICAL1microtubule associated monooxygenase, calponin and LIM domain containing 1 | Pole registreeritud | Esineb 1 haiguses |
| MOCS1molybdenum cofactor synthesis 1 | Pole registreeritud | Esineb 1 haiguses |
| MPDZmultiple PDZ domain crumbs cell polarity complex component | Pole registreeritud | Esineb 1 haiguses |
| MPImannose phosphate isomerase | Pole registreeritud | Esineb 1 haiguses |
| MT-TNmitochondrially encoded tRNA-Asn (AAU/C) | Pole registreeritud | Esineb 1 haiguses |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Pole registreeritud | Esineb 1 haiguses |
| MTR5-methyltetrahydrofolate-homocysteine methyltransferase | Pole registreeritud | Esineb 1 haiguses |
| NANSN-acetylneuraminate synthase | Pole registreeritud | Esineb 1 haiguses |
| NBNnibrin | Pole registreeritud | Esineb 1 haiguses |
| NEDD4LNEDD4 like E3 ubiquitin protein ligase | Pole registreeritud | Esineb 1 haiguses |
| NKX2-5NK2 homeobox 5 | Pole registreeritud | Esineb 1 haiguses |
| NLGN3neuroligin 3 | Pole registreeritud | Esineb 2 haiguses |
| NLGN4Xneuroligin 4 X-linked | Pole registreeritud | Esineb 1 haiguses |
| NOP10NOP10 ribonucleoprotein | Pole registreeritud | Esineb 1 haiguses |
| NPC2NPC intracellular cholesterol transporter 2 | Pole registreeritud | Esineb 1 haiguses |
| NTNG2netrin G2 | Pole registreeritud | Esineb 1 haiguses |
| NUP62nucleoporin 62 | Pole registreeritud | Esineb 1 haiguses |
| OPA1OPA1 mitochondrial dynamin like GTPase | Pole registreeritud | Esineb 1 haiguses |
| OSGEPO-sialoglycoprotein endopeptidase | Pole registreeritud | Esineb 1 haiguses |
| OTCornithine transcarbamylase | Pole registreeritud | Esineb 1 haiguses |
| PAFAH1B1platelet activating factor acetylhydrolase 1b regulatory subunit 1 | Pole registreeritud | Esineb 1 haiguses |
| PAX2paired box 2 | Pole registreeritud | Esineb 1 haiguses |
| PCpyruvate carboxylase | Pole registreeritud | Esineb 1 haiguses |
| PCGF2polycomb group ring finger 2 | Pole registreeritud | Esineb 1 haiguses |
| PDE10Aphosphodiesterase 10A | Pole registreeritud | Esineb 1 haiguses |
| PDHXpyruvate dehydrogenase complex component X | Pole registreeritud | Esineb 1 haiguses |
| PDP1pyruvate dehydrogenase phosphatase catalytic subunit 1 | Pole registreeritud | Esineb 1 haiguses |
| PEX2peroxisomal biogenesis factor 2 | Pole registreeritud | Esineb 1 haiguses |
| PEX5peroxisomal biogenesis factor 5 | Pole registreeritud | Esineb 2 haiguses |
| PEX7peroxisomal biogenesis factor 7 | Pole registreeritud | Esineb 2 haiguses |
| PHGDHphosphoglycerate dehydrogenase | Pole registreeritud | Esineb 1 haiguses |
| PISDphosphatidylserine decarboxylase | Pole registreeritud | Esineb 1 haiguses |
| PITX3paired like homeodomain 3 | Pole registreeritud | Esineb 1 haiguses |
| PLA2G6phospholipase A2 group VI | Pole registreeritud | Esineb 1 haiguses |
| PMPCBpeptidase, mitochondrial processing subunit beta | Pole registreeritud | Esineb 1 haiguses |
| POLR3ARNA polymerase III subunit A | Pole registreeritud | Esineb 1 haiguses |
| PORcytochrome p450 oxidoreductase | Pole registreeritud | Esineb 1 haiguses |
| POU1F1POU class 1 homeobox 1 | Pole registreeritud | Esineb 1 haiguses |
| PPT1palmitoyl-protein thioesterase 1 | Pole registreeritud | Esineb 1 haiguses |
| PRDX1peroxiredoxin 1 | Pole registreeritud | Esineb 1 haiguses |
| PRODH2proline dehydrogenase 2 | Pole registreeritud | Esineb 1 haiguses |
| PTCHD1patched domain containing 1 | Pole registreeritud | Esineb 1 haiguses |
| PTRH2peptidyl-tRNA hydrolase 2 | Pole registreeritud | Esineb 1 haiguses |
| PURApurine rich element binding protein A | Pole registreeritud | Esineb 1 haiguses |
| RBMXRNA binding motif protein X-linked | Pole registreeritud | Esineb 1 haiguses |
| ROGDIrogdi atypical leucine zipper | Pole registreeritud | Esineb 1 haiguses |
| RORARAR related orphan receptor A | Pole registreeritud | Esineb 1 haiguses |
| SACSsacsin molecular chaperone | Pole registreeritud | Esineb 1 haiguses |
| SAR1Bsecretion associated Ras related GTPase 1B | Pole registreeritud | Esineb 1 haiguses |
| SCO1synthesis of cytochrome C oxidase 1 | Pole registreeritud | Esineb 1 haiguses |
| SCO2synthesis of cytochrome C oxidase 2 | Pole registreeritud | Esineb 1 haiguses |
| SETSET nuclear proto-oncogene | Pole registreeritud | Esineb 1 haiguses |
| SF3B2splicing factor 3b subunit 2 | Pole registreeritud | Esineb 1 haiguses |
| SGSHN-sulfoglucosamine sulfohydrolase | Pole registreeritud | Esineb 1 haiguses |
| SLC12A1solute carrier family 12 member 1 | Pole registreeritud | Esineb 1 haiguses |
| SLC12A5solute carrier family 12 member 5 | Pole registreeritud | Esineb 1 haiguses |
| SLC17A5solute carrier family 17 member 5 | Pole registreeritud | Esineb 1 haiguses |
| SLC35A1solute carrier family 35 member A1 | Pole registreeritud | Esineb 1 haiguses |
| SLC35C1solute carrier family 35 member C1 | Pole registreeritud | Esineb 1 haiguses |
| SLC36A2solute carrier family 36 member 2 | Pole registreeritud | Esineb 1 haiguses |
| SLC46A1solute carrier family 46 member 1 | Pole registreeritud | Esineb 1 haiguses |
| SLC9A6solute carrier family 9 member A6 | Pole registreeritud | Esineb 1 haiguses |
| SMARCB1SWI/SNF related BAF chromatin remodeling complex subunit B1 | Pole registreeritud | Esineb 1 haiguses |
| SMARCE1SWI/SNF related BAF chromatin remodeling complex subunit E1 | Pole registreeritud | Esineb 1 haiguses |
| SMOC1SPARC related modular calcium binding 1 | Pole registreeritud | Esineb 1 haiguses |
| SNRPNsmall nuclear ribonucleoprotein polypeptide N | Pole registreeritud | Esineb 1 haiguses |
| ST3GAL3ST3 beta-galactoside alpha-2,3-sialyltransferase 3 | Pole registreeritud | Esineb 1 haiguses |
| STRADASTE20 related adaptor alpha | Pole registreeritud | Esineb 1 haiguses |
| SURF1SURF1 cytochrome c oxidase assembly factor | Pole registreeritud | Esineb 1 haiguses |
| SYNE2spectrin repeat containing nuclear envelope protein 2 | Pole registreeritud | Esineb 1 haiguses |
| TCN2transcobalamin 2 | Pole registreeritud | Esineb 1 haiguses |
| TDP1tyrosyl-DNA phosphodiesterase 1 | Pole registreeritud | Esineb 1 haiguses |
| TENM3teneurin transmembrane protein 3 | Pole registreeritud | Esineb 1 haiguses |
| TGFBR1transforming growth factor beta receptor 1 | Pole registreeritud | Esineb 1 haiguses |
| TK2thymidine kinase 2 | Pole registreeritud | Esineb 1 haiguses |
| TMEM107transmembrane protein 107 | Pole registreeritud | Esineb 1 haiguses |
| TMEM43transmembrane protein 43 | Pole registreeritud | Esineb 1 haiguses |
| TNNT1troponin T1, slow skeletal type | Pole registreeritud | Esineb 1 haiguses |
| TRIT1tRNA isopentenyltransferase 1 | Pole registreeritud | Esineb 1 haiguses |
| TSHBthyroid stimulating hormone subunit beta | Pole registreeritud | Esineb 1 haiguses |
| TUBB4Atubulin beta 4A class IVa | Pole registreeritud | Esineb 1 haiguses |
| TWNKtwinkle mtDNA helicase | Pole registreeritud | Esineb 1 haiguses |
| UFC1ubiquitin-fold modifier conjugating enzyme 1 | Pole registreeritud | Esineb 1 haiguses |
| UFM1ubiquitin fold modifier 1 | Pole registreeritud | Esineb 1 haiguses |
| USP27Xubiquitin specific peptidase 27 X-linked | Pole registreeritud | Esineb 1 haiguses |
| VRK1VRK serine/threonine kinase 1 | Pole registreeritud | Esineb 1 haiguses |
| VWA3Bvon Willebrand factor A domain containing 3B | Pole registreeritud | Esineb 1 haiguses |
| WNK3WNK lysine deficient protein kinase 3 | Pole registreeritud | Esineb 1 haiguses |
| YY1AP1YY1 associated protein 1 | Pole registreeritud | Esineb 1 haiguses |
| ZNF148zinc finger protein 148 | Pole registreeritud | Esineb 1 haiguses |
| ZNF292zinc finger protein 292 | Pole registreeritud | Esineb 1 haiguses |
Kui sageli see esineb geenist tulenevate seisunditega inimeste seas, kõige sagedamini nende kõigi seas, nagu on märgitud Inimese fenotüübi ontoloogias. Need lehed kirjeldavad tunnuseid ja nende taga olevaid uuringuid; need ei ole diagnoos ning sümptomite kohta tuleks küsida arstilt või geneetilt nõustajalt.
Kitsamad tunnused
Laiemad tunnused
Allikas
- Inimese fenotüübi ontoloogia, versioon 2026-09-01: tunnus, selle nimetused, määratlus ja sellega seotud geenid. Lisateave leiab aadressilt hpo.jax.org.
- Andmeversioon 2026.10.18-8b139e39.
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