AtlasKellele me abiks olemeMeie teadusTootedTulemused
Logi sisseKüsiSekveneeri oma genoom↗
Tunnus
Weight loss
Reduction of total body weight.
Kokkuvõte
- Teised nimetused
- Loss of weight
- Kehasüsteem
- Growth abnormality
AtlasKellele me abiks olemeMeie teadusTootedTulemused
Logi sisseKüsiSekveneeri oma genoom↗
Selle lehe andmed
Lehe aadressile saab lisada .json või päringusse application/json, et lugeda seda JSON-vormingus.
library(jsonlite)
url <- "https://dantelabs.com/traits/weight-loss.json"
page <- fromJSON(url)
page$trait$nameWeight lossHP:0001824
AtlasKellele me abiks olemeMeie teadusTootedTulemused
Logi sisseKüsiSekveneeri oma genoom↗
Lugege välja geenid, mis on seotud Weight loss-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test176 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.
- Fanconi AnemiaReads 18 of these genesBRCA1BRCA2PALB2BRIP1ERCC4FANCAAbout this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 20 of these genesDCTN1ANGANXA11CCNFCHCHD10CHMP2BAbout this report →
- DNA Repair DiseaseReads 22 of these genesBRCA1BRCA2MLH1MSH2MSH6PALB2About this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 9 of these genesMAXRETSDHASDHAF2SDHBSDHCAbout this report →
Show 172 more reports
- Malignant Endocrine NeoplasmReads 8 of these genesTP53CDC73CDKN1BMEN1RETSDHAAbout this report →
- Urinary and Renal System TumourReads 8 of these genesTP53BAP1RETSDHASDHAF2SDHBAbout this report →
- Other Inborn Errors of ImmunityReads 33 of these genesPTCRAATMBCL10C4AC4BCR2About this report →
- Lynch SyndromeReads 5 of these genesEPCAMMLH1MSH2MSH6PMS2About this report →
- Inherited Neurodegenerative DisordersReads 41 of these genesABCB7POLGATMDCTN1TREX1ABCD1About this report →
- Familial Glucocorticoid DeficiencyReads 6 of these genesAAASMC2RMRAPNNTTXNRD2NR0B1About this report →
- Frontotemporal DementiaReads 7 of these genesCCNFCHCHD10CHMP2BHNRNPA1SQSTM1TBK1About this report →
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 5 of these genesATMCHEK2PALB2BRIP1RAD51CAbout this report →
- Kidney CancerReads 5 of these genesTP53BAP1SDHBVHLTRIM28About this report →
- Neonatal Diabetes MellitusReads 7 of these genesABCC8GCKINSKCNJ11PDX1GATA4About this report →
- Autoimmune DiseaseReads 7 of these genesCTLA4KRASSTAT3TREX1NOD2STAT1About this report →
- Hereditary Gastrointestinal Stromal TumourReads 3 of these genesKITSDHBSDHCAbout this report →
- Maturity-Onset Diabetes Of The YoungReads 5 of these genesABCC8GCKINSKCNJ11PDX1About this report →
- Hereditary Breast and Ovarian Cancer (BRCA1/2)Reads 2 of these genesBRCA1BRCA2About this report →
- Hereditary Wilms TumourReads 2 of these genesWT1RESTAbout this report →
- Hypercalcemia InfantileReads 2 of these genesSLC34A1CYP24A1About this report →
- Juvenile Polyposis SyndromeReads 2 of these genesBMPR1ASMAD4About this report →
- Neuroblastoma Predisposition (ALK and PHOX2B)Reads 2 of these genesALKPHOX2BAbout this report →
- STAT1 and STAT3 Gain-of-Function DiseaseReads 2 of these genesSTAT3STAT1About this report →
- Mendelian Susceptibility to Mycobacterial Disease (MSMD)Reads 4 of these genesIL12BSTAT1IFNGR1IL23RAbout this report →
- Diabetes MellitusReads 7 of these genesABCC8GCKINSKCNJ11PDX1GATA4About this report →
- Rare Hereditary Peripheral NeuropathiesReads 19 of these genesPOLGTYMPDCTN1LMNAATP7ACHCHD10About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 7 of these genesLPIN2TNFAIP3TREX1ELF4IFIH1PTPN2About this report →
- Disorder of Copper MetabolismReads 2 of these genesATP7BATP7AAbout this report →
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 2 of these genesPHOX2BRETAbout this report →
- Neuroacanthocytosis and Huntington Disease PhenocopiesReads 2 of these genesJPH3VPS13AAbout this report →
- Distal MyopathiesReads 5 of these genesGIPC1LRP12HNRNPA1MATR3VCPAbout this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 3 of these genesCTLA4KRASFASAbout this report →
- Classic Organic AciduriasReads 3 of these genesACAT1HMGCLIVDAbout this report →
- Colorectal Cancer & PolyposisReads 3 of these genesMUTYHPOLD1POLEAbout this report →
- Inherited Predisposition to Acute Myeloid LeukaemiaReads 3 of these genesGATA2RUNX1TERTAbout this report →
- IPEX Syndrome and Other TregopathiesReads 3 of these genesCTLA4IL2RAIL2RBAbout this report →
- Congenital MyopathiesReads 5 of these genesACTA1MAP3K20SELENONTPM2TPM3About this report →
- Aicardi-Goutieres SyndromeReads 3 of these genesTREX1IFIH1RNU7-1About this report →
- Parkinson DiseaseReads 4 of these genesGBA1LRRK2SNCAVPS35About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 6 of these genesGJA1GJB3GJB4KDSRKRT1RHBDF2About this report →
- Fanconi Renotubular Syndrome and Renal GlucosuriaReads 2 of these genesEHHADHGATMAbout this report →
- Alacrima, Achalasia and Intellectual Disability Syndrome (GMPPA)Reads 1 of these genesGMPPAAbout this report →
- Amyotrophic Lateral Sclerosis Susceptibility 24 (NEK1)Reads 1 of these genesNEK1About this report →
- Ataxia-TelangiectasiaReads 1 of these genesATMAbout this report →
- BAP1 Tumour Predisposition SyndromeReads 1 of these genesBAP1About this report →
- Congenital Central Hypoventilation SyndromeReads 1 of these genesPHOX2BAbout this report →
- CTNNB1 SyndromeReads 1 of these genesCTNNB1About this report →
- Curry-Jones Syndrome (Mosaic SMO Syndrome)Reads 1 of these genesSMOAbout this report →
- CystinosisReads 1 of these genesCTNSAbout this report →
- Familial Mediterranean FeverReads 1 of these genesMEFVAbout this report →
- FANCM-Related Genomic Instability DisorderReads 1 of these genesFANCMAbout this report →
- Feingold Syndrome Type 1Reads 1 of these genesMYCNAbout this report →
- Gaucher DiseaseReads 1 of these genesGBA1About this report →
- Genetic Prion Disease (incl. Fatal Familial Insomnia)Reads 1 of these genesPRNPAbout this report →
- Glucose-Galactose MalabsorptionReads 1 of these genesSLC5A1About this report →
- Hereditary Leiomyomatosis and Renal Cell CancerReads 1 of these genesFHAbout this report →
- Hereditary RetinoblastomaReads 1 of these genesRB1About this report →
- Hereditary Thrombocythaemia (JAK2)Reads 1 of these genesJAK2About this report →
- Hereditary Thrombocythaemia (THPO)Reads 1 of these genesTHPOAbout this report →
- Huntington DiseaseReads 1 of these genesHTTAbout this report →
- Krabbe DiseaseReads 1 of these genesGALCAbout this report →
- Li-Fraumeni SyndromeReads 1 of these genesTP53About this report →
- MDPL SyndromeReads 1 of these genesPOLD1About this report →
- MPL-Related Hereditary ThrombocythaemiaReads 1 of these genesMPLAbout this report →
- OPTN-Related Normal-Tension GlaucomaReads 1 of these genesOPTNAbout this report →
- PALB2 related diseasesReads 1 of these genesPALB2About this report →
- PDX1-Related Pancreatic AgenesisReads 1 of these genesPDX1About this report →
- Perlman SyndromeReads 1 of these genesDIS3L2About this report →
- PIK3R1-Related DisordersReads 1 of these genesPIK3R1About this report →
- Pulmonary Alveolar MicrolithiasisReads 1 of these genesSLC34A2About this report →
- Restrictive Dermopathy (ZMPSTE24)Reads 1 of these genesZMPSTE24About this report →
- Rett Syndrome and MECP2-Related DisordersReads 1 of these genesMECP2About this report →
- Simpson-Golabi-Behmel SyndromeReads 1 of these genesGPC3About this report →
- Tylosis with Oesophageal CancerReads 1 of these genesRHBDF2About this report →
- UNC13A-Related Neurodevelopmental DisordersReads 1 of these genesUNC13AAbout this report →
- Von Hippel-Lindau DiseaseReads 1 of these genesVHLAbout this report →
- Wilson DiseaseReads 1 of these genesATP7BAbout this report →
- X-Linked Adrenoleukodystrophy (ABCD1)Reads 1 of these genesABCD1About this report →
- Common Variable Immunodeficiency (Monogenic CVID)Reads 3 of these genesCR2IKZF1IRF2BP2About this report →
- HyperinsulinismReads 3 of these genesABCC8GCKKCNJ11About this report →
- PancreatitisReads 2 of these genesCTRCSPINK1About this report →
- Inherited ThrombocytopeniasReads 5 of these genesKDSRRUNX1FLI1MPLTHPOAbout this report →
- Noonan SyndromeReads 4 of these genesKRASCBLMAP2K1NRASAbout this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 2 of these genesFLNAERBB3About this report →
- Other Inherited LeukodystrophiesReads 7 of these genesTREX1ABCD1TREM2GALCIFIH1PSAPAbout this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 3 of these genesSCNN1ASCNN1BSCNN1GAbout this report →
- Hyper-IgE SyndromeReads 2 of these genesSTAT3STAT6About this report →
- Waardenburg SyndromeReads 2 of these genesEDN3EDNRBAbout this report →
- Thyroid CancerReads 4 of these genesTSHRCDC73MEN1RETAbout this report →
- PolycythemiaReads 2 of these genesEPAS1VHLAbout this report →
- Acrodermatitis EnteropathicaReads 1 of these genesSLC39A4About this report →
- Activated PI3K-Delta Syndrome (APDS)Reads 1 of these genesPIK3R1About this report →
- Biotinidase & Holocarboxylase DeficiencyReads 1 of these genesHLCSAbout this report →
- Hereditary Gingival FibromatosisReads 1 of these genesRESTAbout this report →
- Hereditary Mixed Polyposis SyndromeReads 1 of these genesBMPR1AAbout this report →
- Malignant Hyperthermia SusceptibilityReads 1 of these genesCACNA1SAbout this report →
- Metachromatic LeukodystrophyReads 1 of these genesPSAPAbout this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 3 of these genesATRXGATA4WT1About this report →
- Female InfertilityReads 5 of these genesATMSTARFANCMTRIP13TWNKAbout this report →
- Charcot-Marie-Tooth DiseaseReads 6 of these genesDCTN1LMNAATP7AFIG4NEFHVCPAbout this report →
- Lysosomal Storage DiseaseReads 5 of these genesCTNSGALCGBA1GNPTABPSAPAbout this report →
- Hypertrophic CardiomyopathyReads 5 of these genesKRASMYL2H19MAP2K1NRASAbout this report →
- Agammaglobulinaemia (XLA and Autosomal Forms)Reads 2 of these genesPIK3R1BTKAbout this report →
- Intellectual DisabilityReads 9 of these genesFOXP1MECP2SMAD4ASXL1ATRXCTNNB1About this report →
- Hereditary AmyloidosisReads 2 of these genesB2MTTRAbout this report →
- LipodystrophyReads 2 of these genesLMNAZMPSTE24About this report →
- Type I InterferonopathiesReads 2 of these genesTREX1IFIH1About this report →
- Alport SyndromeReads 1 of these genesCOL4A5About this report →
- Cerebral Creatine Deficiency SyndromesReads 1 of these genesGATMAbout this report →
- Familial Periodic ParalysisReads 1 of these genesCACNA1SAbout this report →
- HyperthyroidismReads 1 of these genesTSHRAbout this report →
- Mucolipidoses (ML II, ML III and ML IV)Reads 1 of these genesGNPTABAbout this report →
- Spinal Muscular AtrophyReads 3 of these genesDCTN1ATP7ACHCHD10About this report →
- Congenital Diarrhoeas & EnteropathiesReads 2 of these genesEPCAMSLC5A1About this report →
- Inherited Congenital Heart DefectsReads 2 of these genesFLNAGATA4About this report →
- Severe Combined ImmunodeficiencyReads 3 of these genesAK2CD247CIITAAbout this report →
- Primary Mitochondrial DiseaseReads 6 of these genesPOLGTYMPLIG3NDUFAF6RRM2BTWNKAbout this report →
- Adult-Onset Leukodystrophies (CSF1R, LMNB1, Nasu-Hakola)Reads 1 of these genesTREM2About this report →
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 1 of these genesPRKAR1AAbout this report →
- Congenital Dyserythropoietic AnaemiasReads 1 of these genesKLF1About this report →
- Familial Paget Disease of BoneReads 1 of these genesSQSTM1About this report →
- Hereditary Hemorrhagic TelangiectasiaReads 1 of these genesSMAD4About this report →
- Inherited Predisposition to Myeloid Blood CancersReads 1 of these genesGATA2About this report →
- MelanomaReads 1 of these genesCDKN2AAbout this report →
- NeurofibromatosisReads 1 of these genesNF1About this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesDNMT3AAbout this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 1 of these genesPRKAR1AAbout this report →
- Inherited Complement and Properdin DeficienciesReads 2 of these genesC4AC4BAbout this report →
- Homocystinuria & Cobalamin DisordersReads 2 of these genesAMNCUBNAbout this report →
- Alzheimer diseaseReads 1 of these genesTREM2About this report →
- Chronic Mucocutaneous CandidiasisReads 1 of these genesSTAT1About this report →
- Mosaic Variegated Aneuploidy SyndromeReads 1 of these genesTRIP13About this report →
- MTOR Pathway Megalencephaly and Overgrowth DisordersReads 1 of these genesPIK3CAAbout this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Dyskeratosis CongenitaReads 2 of these genesNPM1TERTAbout this report →
- Inherited IchthyosesReads 2 of these genesKRT1KRT10About this report →
- Growth Hormone Insensitivity & IGF-1 Axis DisordersReads 1 of these genesSTAT5BAbout this report →
- HemochromatosisReads 1 of these genesHFEAbout this report →
- Inflammatory Bowel Diseases (IBD)Reads 1 of these genesIL10About this report →
- Loeys-Dietz SyndromeReads 1 of these genesTGFBR2About this report →
- Systemic Lupus ErythematosusReads 1 of these genesTREX1About this report →
- Congenital Adrenal HyperplasiaReads 1 of these genesSTARAbout this report →
- Inherited Parathyroid & Calcium-Sensing DisordersReads 1 of these genesCDC73About this report →
- Congenital Muscular DystrophiesReads 2 of these genesITGA7SELENONAbout this report →
- Epilepsy (Full Panel)Reads 5 of these genesFLNAMECP2GABRA3HACE1MDH2About this report →
- GlaucomaReads 1 of these genesOPTNAbout this report →
- Hereditary Sideroblastic AnaemiasReads 1 of these genesABCB7About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Limb-Girdle Muscular DystrophyReads 2 of these genesLMNATRAPPC11About this report →
- Familial Pulmonary FibrosisReads 1 of these genesTERTAbout this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 1 of these genesH19About this report →
- ThrombophiliaReads 1 of these genesF5About this report →
- Marfan Like SyndromesReads 1 of these genesTGFBR2About this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 1 of these genesPANK2About this report →
- Rare Inherited Coagulation Factor DeficienciesReads 1 of these genesF5About this report →
- Polycystic Kidney DiseaseReads 1 of these genesPKHD1About this report →
- Usher SyndromeReads 1 of these genesCDH23About this report →
- Aortic AneurysmReads 1 of these genesTGFBR2About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 2 of these genesRNF168TWNKAbout this report →
- Cutis LaxaReads 1 of these genesATP7AAbout this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 1 of these genesHMGCLAbout this report →
- Hereditary Spastic ParaplegiaReads 2 of these genesABCD1HACE1About this report →
- Leigh SyndromeReads 2 of these genesNDUFAF6SDHAAbout this report →
- Hereditary Corneal DystrophiesReads 1 of these genesTCF4About this report →
- Congenital HypothyroidismReads 1 of these genesTSHRAbout this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 1 of these genesCRLF1About this report →
- Syndromic CraniosynostosisReads 1 of these genesSMOAbout this report →
- Hearing Loss and DeafnessReads 2 of these genesCDH23COL4A6About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesSMOAbout this report →
- VitreoretinopathyReads 1 of these genesCTNNB1About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesBCORAbout this report →
- Osteogenesis ImperfectaReads 1 of these genesIFIH1About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesATXN2About this report →
- Male InfertilityReads 1 of these genesFANCMAbout this report →
- Dilated CardiomyopathyReads 1 of these genesLMNAAbout this report →
- Hypogonadotropic HypogonadismReads 1 of these genesNR0B1About this report →
Lugege välja geenid, mis on seotud Weight loss-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test353 geeni on seotud tunnusega Weight loss
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Weight loss. 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 |
|---|---|---|
| ABCB7ATP binding cassette subfamily B member 7 | Alati | Esineb 1 haiguses |
| CTNScystinosin, lysosomal cystine transporter | Alati | Esineb 1 haiguses |
| FLNAfilamin A | Alati | Esineb 1 haiguses |
| KCNJ18potassium inwardly rectifying channel subfamily J member 18 | Alati | Esineb 2 haiguses |
| KLF1KLF transcription factor 1 | Alati | Esineb 1 haiguses |
| POLGDNA polymerase gamma, catalytic subunit | Alati | Esineb 4 haiguses |
| PTCRApre T cell antigen receptor alpha | Alati | Esineb 1 haiguses |
| TYMPthymidine phosphorylase | Alati | Esineb 2 haiguses |
| ABCC8ATP binding cassette subfamily C member 8 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ABCD3ATP binding cassette subfamily D member 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ATMATM serine/threonine kinase | Väga sageli (80–99%) | Esineb 2 haiguses |
| ATP7BATPase copper transporting beta | Väga sageli (80–99%) | Esineb 1 haiguses |
| BANK1B cell scaffold protein with ankyrin repeats 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| BCL10BCL10 immune signaling adaptor | Väga sageli (80–99%) | Esineb 1 haiguses |
| BCL2BCL2 apoptosis regulator | Väga sageli (80–99%) | Esineb 1 haiguses |
| BCL6BCL6 transcription repressor | Väga sageli (80–99%) | Esineb 1 haiguses |
| BIRC3baculoviral IAP repeat containing 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| BLKBLK proto-oncogene, Src family tyrosine kinase | Väga sageli (80–99%) | Esineb 1 haiguses |
| BMPR1Abone morphogenetic protein receptor type 1A | Väga sageli (80–99%) | Esineb 1 haiguses |
| BRCA1BRCA1 DNA repair associated | Väga sageli (80–99%) | Esineb 2 haiguses |
| BRCA2BRCA2 DNA repair associated | Väga sageli (80–99%) | Esineb 4 haiguses |
| C4Acomplement C4A (Chido/Rodgers blood group) | Väga sageli (80–99%) | Esineb 2 haiguses |
| C4Bcomplement C4B (Chido/Rodgers blood group) | Väga sageli (80–99%) | Esineb 1 haiguses |
| CDKN2Acyclin dependent kinase inhibitor 2A | Väga sageli (80–99%) | Esineb 2 haiguses |
| CHEK2checkpoint kinase 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| CR2complement C3d receptor 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Väga sageli (80–99%) | Esineb 3 haiguses |
| DCTN1dynactin subunit 1 | Väga sageli (80–99%) | Esineb 3 haiguses |
| DNASE1deoxyribonuclease 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| EPCAMepithelial cell adhesion molecule | Väga sageli (80–99%) | Esineb 2 haiguses |
| ETS1ETS proto-oncogene 1, transcription factor | Väga sageli (80–99%) | Esineb 1 haiguses |
| FCGR2BFc gamma receptor IIb | Väga sageli (80–99%) | Esineb 1 haiguses |
| FCGR3BFc gamma receptor IIIb | Väga sageli (80–99%) | Esineb 1 haiguses |
| FOXP1forkhead box P1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| GCKglucokinase | Väga sageli (80–99%) | Esineb 1 haiguses |
| GIPC1GIPC PDZ domain containing family member 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| GJA1gap junction protein alpha 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| GJB3gap junction protein beta 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| GJB4gap junction protein beta 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| HLA-Bmajor histocompatibility complex, class I, B | Väga sageli (80–99%) | Esineb 5 haiguses |
Näita veel 313 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| HLA-DPA1major histocompatibility complex, class II, DP alpha 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| HLA-DPB1major histocompatibility complex, class II, DP beta 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Väga sageli (80–99%) | Esineb 3 haiguses |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Väga sageli (80–99%) | Esineb 7 haiguses |
| HLCSholocarboxylase synthetase | Väga sageli (80–99%) | Esineb 1 haiguses |
| IGHimmunoglobulin heavy locus | Väga sageli (80–99%) | Esineb 3 haiguses |
| IGHG1immunoglobulin heavy constant gamma 1 (G1m marker) | Väga sageli (80–99%) | Esineb 1 haiguses |
| IKZF1IKAROS family zinc finger 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| IL10interleukin 10 | Väga sageli (80–99%) | Esineb 3 haiguses |
| IL12Binterleukin 12B | Väga sageli (80–99%) | Esineb 1 haiguses |
| INSinsulin | Väga sageli (80–99%) | Esineb 1 haiguses |
| IRAK1interleukin 1 receptor associated kinase 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| IRF5interferon regulatory factor 5 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ITGAMintegrin subunit alpha M | Väga sageli (80–99%) | Esineb 1 haiguses |
| JAK2Janus kinase 2 | Väga sageli (80–99%) | Esineb 3 haiguses |
| JAZF1JAZF zinc finger 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| KCNJ11potassium inwardly rectifying channel subfamily J member 11 | Väga sageli (80–99%) | Esineb 1 haiguses |
| KDSR3-ketodihydrosphingosine reductase | Väga sageli (80–99%) | Esineb 1 haiguses |
| KIAA0319LKIAA0319 like | Väga sageli (80–99%) | Esineb 1 haiguses |
| KRASKRas proto-oncogene, GTPase | Väga sageli (80–99%) | Esineb 2 haiguses |
| KRT1keratin 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| KRT10keratin 10 | Väga sageli (80–99%) | Esineb 1 haiguses |
| LMNAlamin A/C | Väga sageli (80–99%) | Esineb 1 haiguses |
| LPIN2lipin 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| LRP12LDL receptor related protein 12 | Väga sageli (80–99%) | Esineb 3 haiguses |
| MALT1MALT1 paracaspase | Väga sageli (80–99%) | Esineb 1 haiguses |
| MECP2methyl-CpG binding protein 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| MLH1mutL homolog 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| MLXMAX dimerization protein MLX | Väga sageli (80–99%) | Esineb 1 haiguses |
| MSH2mutS homolog 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| MSH6mutS homolog 6 | Väga sageli (80–99%) | Esineb 1 haiguses |
| MUTYHmutY DNA glycosylase | Väga sageli (80–99%) | Esineb 1 haiguses |
| NOTCH2NLCnotch 2 N-terminal like C | Väga sageli (80–99%) | Esineb 1 haiguses |
| NPATnuclear protein, coactivator of histone transcription | Väga sageli (80–99%) | Esineb 1 haiguses |
| NUTM2B-AS1NUTM2B antisense RNA 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| P4HA2prolyl 4-hydroxylase subunit alpha 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PALB2partner and localizer of BRCA2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| PALLDpalladin, cytoskeletal associated protein | Väga sageli (80–99%) | Esineb 1 haiguses |
| PDCD1programmed cell death 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PDX1pancreatic and duodenal homeobox 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Väga sageli (80–99%) | Esineb 1 haiguses |
| PMS1PMS1 homolog 1, mismatch repair system component | Väga sageli (80–99%) | Esineb 1 haiguses |
| PMS2PMS1 homolog 2, mismatch repair system component | Väga sageli (80–99%) | Esineb 1 haiguses |
| POLD1DNA polymerase delta 1, catalytic subunit | Väga sageli (80–99%) | Esineb 1 haiguses |
| POLEDNA polymerase epsilon, catalytic subunit | Väga sageli (80–99%) | Esineb 1 haiguses |
| PRTN3proteinase 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Väga sageli (80–99%) | Esineb 4 haiguses |
| PXKPX domain containing serine/threonine kinase like | Väga sageli (80–99%) | Esineb 1 haiguses |
| RABL3RAB, member of RAS oncogene family like 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| RILPL1Rab interacting lysosomal protein like 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| RPS20ribosomal protein S20 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SEMA4Asemaphorin 4A | Väga sageli (80–99%) | Esineb 1 haiguses |
| SLC5A1solute carrier family 5 member 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SMAD4SMAD family member 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SPP1secreted phosphoprotein 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| STAT3signal transducer and activator of transcription 3 | Väga sageli (80–99%) | Esineb 2 haiguses |
| STAT4signal transducer and activator of transcription 4 | Väga sageli (80–99%) | Esineb 3 haiguses |
| TGFBR2transforming growth factor beta receptor 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TLR7toll like receptor 7 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TNFAIP3TNF alpha induced protein 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TNFSF4TNF superfamily member 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TNIP1TNFAIP3 interacting protein 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TP53tumor protein p53 | Väga sageli (80–99%) | Esineb 3 haiguses |
| TREX1three prime repair exonuclease 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TSHRthyroid stimulating hormone receptor | Väga sageli (80–99%) | Esineb 2 haiguses |
| UBE2L3ubiquitin conjugating enzyme E2 L3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ZMPSTE24zinc metallopeptidase STE24 | Väga sageli (80–99%) | Esineb 1 haiguses |
| AAASaladin WD repeat nucleoporin | Sageli (30–79%) | Esineb 1 haiguses |
| ABCD1ATP binding cassette subfamily D member 1 | Sageli (30–79%) | Esineb 1 haiguses |
| ACTA1actin alpha 1, skeletal muscle | Sageli (30–79%) | Esineb 1 haiguses |
| AK2adenylate kinase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| ALKALK receptor tyrosine kinase | Sageli (30–79%) | Esineb 1 haiguses |
| ANGangiogenin | Sageli (30–79%) | Esineb 1 haiguses |
| ANO1anoctamin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| ANXA11annexin A11 | Sageli (30–79%) | Esineb 1 haiguses |
| ASXL1ASXL transcriptional regulator 1 | Sageli (30–79%) | Esineb 2 haiguses |
| ATP7AATPase copper transporting alpha | Sageli (30–79%) | Esineb 1 haiguses |
| ATRXATRX chromatin remodeler | Sageli (30–79%) | Esineb 1 haiguses |
| ATXN2ataxin 2 | Sageli (30–79%) | Esineb 1 haiguses |
| AVParginine vasopressin | Sageli (30–79%) | Esineb 1 haiguses |
| B2Mbeta-2-microglobulin | Sageli (30–79%) | Esineb 1 haiguses |
| BAP1BRCA1 associated deubiquitinase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| BCORBCL6 corepressor | Sageli (30–79%) | Esineb 1 haiguses |
| BTNL2butyrophilin like 2 | Sageli (30–79%) | Esineb 1 haiguses |
| CACNA1Scalcium voltage-gated channel subunit alpha1 S | Sageli (30–79%) | Esineb 2 haiguses |
| CBLCbl proto-oncogene | Sageli (30–79%) | Esineb 1 haiguses |
| CCND1cyclin D1 | Sageli (30–79%) | Esineb 2 haiguses |
| CCNFcyclin F | Sageli (30–79%) | Esineb 1 haiguses |
| CDC73cell division cycle 73 | Sageli (30–79%) | Esineb 1 haiguses |
| CDH23cadherin related 23 | Sageli (30–79%) | Esineb 1 haiguses |
| CDKN1Bcyclin dependent kinase inhibitor 1B | Sageli (30–79%) | Esineb 1 haiguses |
| CDKN2Bcyclin dependent kinase inhibitor 2B | Sageli (30–79%) | Esineb 1 haiguses |
| CFAP410cilia and flagella associated protein 410 | Sageli (30–79%) | Esineb 1 haiguses |
| CHCHD10coiled-coil-helix-coiled-coil-helix domain containing 10 | Sageli (30–79%) | Esineb 1 haiguses |
| CHMP2Bcharged multivesicular body protein 2B | Sageli (30–79%) | Esineb 1 haiguses |
| CRLF1cytokine receptor like factor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CTNNB1catenin beta 1 | Sageli (30–79%) | Esineb 1 haiguses |
| DAOD-amino acid oxidase | Sageli (30–79%) | Esineb 1 haiguses |
| DLSTdihydrolipoamide S-succinyltransferase | Sageli (30–79%) | Esineb 1 haiguses |
| DNMT3ADNA methyltransferase 3 alpha | Sageli (30–79%) | Esineb 1 haiguses |
| ECE1endothelin converting enzyme 1 | Sageli (30–79%) | Esineb 1 haiguses |
| EDN3endothelin 3 | Sageli (30–79%) | Esineb 1 haiguses |
| EDNRBendothelin receptor type B | Sageli (30–79%) | Esineb 1 haiguses |
| EHHADHenoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase | Sageli (30–79%) | Esineb 1 haiguses |
| ELF4E74 like ETS transcription factor 4 | Sageli (30–79%) | Esineb 1 haiguses |
| EPAS1endothelial PAS domain protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| ERBB2erb-b2 receptor tyrosine kinase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| ERBB3erb-b2 receptor tyrosine kinase 3 | Sageli (30–79%) | Esineb 1 haiguses |
| ERBB4erb-b2 receptor tyrosine kinase 4 | Sageli (30–79%) | Esineb 1 haiguses |
| EWSR1EWS RNA binding protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| FHfumarate hydratase | Sageli (30–79%) | Esineb 1 haiguses |
| FIG4FIG4 phosphoinositide 5-phosphatase | Sageli (30–79%) | Esineb 1 haiguses |
| FIP1L1factor interacting with PAPOLA and CPSF1 | Sageli (30–79%) | Esineb 1 haiguses |
| FUSFUS RNA binding protein | Sageli (30–79%) | Esineb 1 haiguses |
| GABRA3gamma-aminobutyric acid type A receptor subunit alpha3 | Sageli (30–79%) | Esineb 1 haiguses |
| GATA2GATA binding protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| GATA4GATA binding protein 4 | Sageli (30–79%) | Esineb 1 haiguses |
| GATMglycine amidinotransferase | Sageli (30–79%) | Esineb 1 haiguses |
| GDNFglial cell derived neurotrophic factor | Sageli (30–79%) | Esineb 1 haiguses |
| GLE1GLE1 RNA export mediator | Sageli (30–79%) | Esineb 1 haiguses |
| GLT8D1glycosyltransferase 8 domain containing 1 | Sageli (30–79%) | Esineb 1 haiguses |
| GMPPAGDP-mannose pyrophosphorylase A | Sageli (30–79%) | Esineb 1 haiguses |
| GPR35G protein-coupled receptor 35 | Sageli (30–79%) | Esineb 1 haiguses |
| HACD13-hydroxyacyl-CoA dehydratase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| HACE1HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| HAVCR2hepatitis A virus cellular receptor 2 | Sageli (30–79%) | Esineb 1 haiguses |
| HLA-DQA1major histocompatibility complex, class II, DQ alpha 1 | Sageli (30–79%) | Esineb 2 haiguses |
| HNRNPA1heterogeneous nuclear ribonucleoprotein A1 | Sageli (30–79%) | Esineb 1 haiguses |
| HTThuntingtin | Sageli (30–79%) | Esineb 2 haiguses |
| IRF2BP2interferon regulatory factor 2 binding protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| ITGA7integrin subunit alpha 7 | Sageli (30–79%) | Esineb 1 haiguses |
| KIF1Bkinesin family member 1B | Sageli (30–79%) | Esineb 2 haiguses |
| KITKIT proto-oncogene, receptor tyrosine kinase | Sageli (30–79%) | Esineb 1 haiguses |
| LIG3DNA ligase 3 | Sageli (30–79%) | Esineb 1 haiguses |
| LIN28Blin-28 RNA binding posttranscriptional regulator B | Sageli (30–79%) | Esineb 1 haiguses |
| LMO1LIM domain only 1 | Sageli (30–79%) | Esineb 1 haiguses |
| MAP3K20mitogen-activated protein kinase kinase kinase 20 | Sageli (30–79%) | Esineb 1 haiguses |
| MATR3matrin 3 | Sageli (30–79%) | Esineb 1 haiguses |
| MAXMYC associated transcriptional regulator X | Sageli (30–79%) | Esineb 1 haiguses |
| MC2Rmelanocortin 2 receptor | Sageli (30–79%) | Esineb 1 haiguses |
| MDH2malate dehydrogenase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| MEN1menin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| MRAPmelanocortin 2 receptor accessory protein | Sageli (30–79%) | Esineb 1 haiguses |
| MST1macrophage stimulating 1 | Sageli (30–79%) | Esineb 1 haiguses |
| MYCNMYCN proto-oncogene, bHLH transcription factor | Sageli (30–79%) | Esineb 1 haiguses |
| MYL2myosin light chain 2 | Sageli (30–79%) | Esineb 1 haiguses |
| NABP1nucleic acid binding protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NDUFAF6NADH:ubiquinone oxidoreductase complex assembly factor 6 | Sageli (30–79%) | Esineb 1 haiguses |
| NEFHneurofilament heavy chain | Sageli (30–79%) | Esineb 1 haiguses |
| NEK1NIMA related kinase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NF1neurofibromin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NNTnicotinamide nucleotide transhydrogenase | Sageli (30–79%) | Esineb 1 haiguses |
| NOD2nucleotide binding oligomerization domain containing 2 | Sageli (30–79%) | Esineb 2 haiguses |
| NOS1nitric oxide synthase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NPM1nucleophosmin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NRTNneurturin | Sageli (30–79%) | Esineb 1 haiguses |
| NUMA1nuclear mitotic apparatus protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| OPTNoptineurin | Sageli (30–79%) | Esineb 1 haiguses |
| PFN1profilin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PHOX2Bpaired like homeobox 2B | Sageli (30–79%) | Esineb 1 haiguses |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PMLPML nuclear body scaffold | Sageli (30–79%) | Esineb 1 haiguses |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Sageli (30–79%) | Esineb 2 haiguses |
| PRPHperipherin | Sageli (30–79%) | Esineb 1 haiguses |
| RARAretinoic acid receptor alpha | Sageli (30–79%) | Esineb 1 haiguses |
| RETret proto-oncogene | Sageli (30–79%) | Esineb 3 haiguses |
| RHBDF2rhomboid 5 homolog 2 | Sageli (30–79%) | Esineb 1 haiguses |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Sageli (30–79%) | Esineb 2 haiguses |
| RUNX1RUNX family transcription factor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Sageli (30–79%) | Esineb 3 haiguses |
| SDHAF1succinate dehydrogenase complex assembly factor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SDHAF2succinate dehydrogenase complex assembly factor 2 | Sageli (30–79%) | Esineb 1 haiguses |
| SDHBsuccinate dehydrogenase complex iron sulfur subunit B | Sageli (30–79%) | Esineb 4 haiguses |
| SDHCsuccinate dehydrogenase complex subunit C | Sageli (30–79%) | Esineb 2 haiguses |
| SDHDsuccinate dehydrogenase complex subunit D | Sageli (30–79%) | Esineb 4 haiguses |
| SELENONselenoprotein N | Sageli (30–79%) | Esineb 1 haiguses |
| SEMA3Csemaphorin 3C | Sageli (30–79%) | Esineb 1 haiguses |
| SEMA3Dsemaphorin 3D | Sageli (30–79%) | Esineb 1 haiguses |
| SEMA4Dsemaphorin 4D | Sageli (30–79%) | Esineb 1 haiguses |
| SLC25A11solute carrier family 25 member 11 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC2A3solute carrier family 2 member 3 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC34A1solute carrier family 34 member 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SMOsmoothened, frizzled class receptor | Sageli (30–79%) | Esineb 1 haiguses |
| SOD1superoxide dismutase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SQSTM1sequestosome 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SREBF1sterol regulatory element binding transcription factor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SRSF2serine and arginine rich splicing factor 2 | Sageli (30–79%) | Esineb 2 haiguses |
| STARsteroidogenic acute regulatory protein | Sageli (30–79%) | Esineb 1 haiguses |
| STAT1signal transducer and activator of transcription 1 | Sageli (30–79%) | Esineb 1 haiguses |
| STAT5Bsignal transducer and activator of transcription 5B | Sageli (30–79%) | Esineb 1 haiguses |
| SYKspleen associated tyrosine kinase | Sageli (30–79%) | Esineb 1 haiguses |
| TAF15TATA-box binding protein associated factor 15 | Sageli (30–79%) | Esineb 1 haiguses |
| TARDBPTAR DNA binding protein | Sageli (30–79%) | Esineb 1 haiguses |
| TBK1TANK binding kinase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TBL1XR1TBL1X/Y related 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TCF4transcription factor 4 | Sageli (30–79%) | Esineb 1 haiguses |
| TERTtelomerase reverse transcriptase | Sageli (30–79%) | Esineb 1 haiguses |
| TET2tet methylcytosine dioxygenase 2 | Sageli (30–79%) | Esineb 2 haiguses |
| TMEM127transmembrane protein 127 | Sageli (30–79%) | Esineb 1 haiguses |
| TPM2tropomyosin 2 | Sageli (30–79%) | Esineb 1 haiguses |
| TPM3tropomyosin 3 | Sageli (30–79%) | Esineb 1 haiguses |
| TRAPPC11trafficking protein particle complex subunit 11 | Sageli (30–79%) | Esineb 1 haiguses |
| TREM2triggering receptor expressed on myeloid cells 2 | Sageli (30–79%) | Esineb 1 haiguses |
| TTRtransthyretin | Sageli (30–79%) | Esineb 1 haiguses |
| TXNRD2thioredoxin reductase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| UBQLN2ubiquilin 2 | Sageli (30–79%) | Esineb 1 haiguses |
| UNC13Aunc-13 homolog A | Sageli (30–79%) | Esineb 1 haiguses |
| VAPBVAMP associated protein B and C | Sageli (30–79%) | Esineb 1 haiguses |
| VCPvalosin containing protein | Sageli (30–79%) | Esineb 1 haiguses |
| VHLvon Hippel-Lindau tumor suppressor | Sageli (30–79%) | Esineb 2 haiguses |
| WT1WT1 transcription factor | Sageli (30–79%) | Esineb 2 haiguses |
| ZBTB16zinc finger and BTB domain containing 16 | Sageli (30–79%) | Esineb 1 haiguses |
| ZNRF3zinc and ring finger 3 | Sageli (30–79%) | Esineb 1 haiguses |
| ACAT1acetyl-CoA acetyltransferase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| AMNamnion associated transmembrane protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| ANKRD55ankyrin repeat domain 55 | Mõnikord (5–29%) | Esineb 1 haiguses |
| BMP6bone morphogenetic protein 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| BRIP1BRCA1 interacting DNA helicase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| BTKBruton tyrosine kinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| CALRcalreticulin | Mõnikord (5–29%) | Esineb 1 haiguses |
| CCR1C-C motif chemokine receptor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CD247CD247 molecule | Mõnikord (5–29%) | Esineb 1 haiguses |
| COL4A5collagen type IV alpha 5 chain | Mõnikord (5–29%) | Esineb 1 haiguses |
| COL4A6collagen type IV alpha 6 chain | Mõnikord (5–29%) | Esineb 1 haiguses |
| CTR9CTR9 component of Paf1/RNA polymerase II complex | Mõnikord (5–29%) | Esineb 1 haiguses |
| CTRCchymotrypsin C | Mõnikord (5–29%) | Esineb 1 haiguses |
| CUBNcubilin | Mõnikord (5–29%) | Esineb 1 haiguses |
| DIS3L2DIS3 like 3'-5' exoribonuclease 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DNAJC13DnaJ heat shock protein family (Hsp40) member C13 | Mõnikord (5–29%) | Esineb 1 haiguses |
| EIF4G1eukaryotic translation initiation factor 4 gamma 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ERAP1endoplasmic reticulum aminopeptidase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| F5coagulation factor V | Mõnikord (5–29%) | Esineb 1 haiguses |
| FAAP100FA core complex associated protein 100 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCAFA complementation group A | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCBFA complementation group B | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCCFA complementation group C | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCD2FA complementation group D2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCEFA complementation group E | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCFFA complementation group F | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCGFA complementation group G | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCIFA complementation group I | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCLFA complementation group L | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCMFA complementation group M | Mõnikord (5–29%) | Esineb 1 haiguses |
| FASFas cell surface death receptor | Mõnikord (5–29%) | Esineb 1 haiguses |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Mõnikord (5–29%) | Esineb 1 haiguses |
| GALCgalactosylceramidase | Mõnikord (5–29%) | Esineb 1 haiguses |
| GBA1glucosylceramidase beta 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GIGYF2GRB10 interacting GYF protein 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Mõnikord (5–29%) | Esineb 1 haiguses |
| GPC3glypican 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| H19H19 imprinted maternally expressed transcript | Mõnikord (5–29%) | Esineb 1 haiguses |
| HFEhomeostatic iron regulator | Mõnikord (5–29%) | Esineb 1 haiguses |
| HMGCL3-hydroxy-3-methylglutaryl-CoA lyase | Mõnikord (5–29%) | Esineb 1 haiguses |
| IFIH1interferon induced with helicase C domain 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IFNGR1interferon gamma receptor 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| IL12Ainterleukin 12A | Mõnikord (5–29%) | Esineb 1 haiguses |
| IL12A-AS1IL12A antisense RNA 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IL23Rinterleukin 23 receptor | Mõnikord (5–29%) | Esineb 1 haiguses |
| IL2RAinterleukin 2 receptor subunit alpha | Mõnikord (5–29%) | Esineb 1 haiguses |
| IL2RBinterleukin 2 receptor subunit beta | Mõnikord (5–29%) | Esineb 1 haiguses |
| IVDisovaleryl-CoA dehydrogenase | Mõnikord (5–29%) | Esineb 1 haiguses |
| JPH3junctophilin 3 | Mõnikord (5–29%) | Esineb 2 haiguses |
| KLRC4killer cell lectin like receptor C4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LRRK2leucine rich repeat kinase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAD2L2mitotic arrest deficient 2 like 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAP2K1mitogen-activated protein kinase kinase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MEFVMEFV innate immunity regulator, pyrin | Mõnikord (5–29%) | Esineb 1 haiguses |
| MPLMPL proto-oncogene, thrombopoietin receptor | Mõnikord (5–29%) | Esineb 1 haiguses |
| NAB2NGFI-A binding protein 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NR0B1nuclear receptor subfamily 0 group B member 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NRASNRAS proto-oncogene, GTPase | Mõnikord (5–29%) | Esineb 1 haiguses |
| PANK2pantothenate kinase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PKHD1PKHD1 ciliary IPT domain containing fibrocystin/polyductin | Mõnikord (5–29%) | Esineb 1 haiguses |
| POU6F2POU class 6 homeobox 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRNPprion protein (Kanno blood group) | Mõnikord (5–29%) | Esineb 4 haiguses |
| PSAPprosaposin | Mõnikord (5–29%) | Esineb 1 haiguses |
| PTPN2protein tyrosine phosphatase non-receptor type 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RAD51RAD51 recombinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| RAD51CRAD51 paralog C | Mõnikord (5–29%) | Esineb 1 haiguses |
| RESTRE1 silencing transcription factor | Mõnikord (5–29%) | Esineb 1 haiguses |
| RFWD3ring finger and WD repeat domain 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RNF168ring finger protein 168 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RNU7-1RNA, U7 small nuclear 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SCNN1Asodium channel epithelial 1 subunit alpha | Mõnikord (5–29%) | Esineb 1 haiguses |
| SCNN1Bsodium channel epithelial 1 subunit beta | Mõnikord (5–29%) | Esineb 1 haiguses |
| SCNN1Gsodium channel epithelial 1 subunit gamma | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC34A2solute carrier family 34 member 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC39A4solute carrier family 39 member 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLX4SLX4 structure-specific endonuclease subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| SNCAsynuclein alpha | Mõnikord (5–29%) | Esineb 2 haiguses |
| SPINK1serine peptidase inhibitor Kazal type 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| STAT6signal transducer and activator of transcription 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| THPOthrombopoietin | Mõnikord (5–29%) | Esineb 1 haiguses |
| TLR4toll like receptor 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TRIM28tripartite motif containing 28 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TRIP13thyroid hormone receptor interactor 13 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TWNKtwinkle mtDNA helicase | Mõnikord (5–29%) | Esineb 1 haiguses |
| UBAC2UBA domain containing 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| UBE2Tubiquitin conjugating enzyme E2 T | Mõnikord (5–29%) | Esineb 1 haiguses |
| UNC45Aunc-45 myosin chaperone A | Mõnikord (5–29%) | Esineb 1 haiguses |
| VPS13Avacuolar protein sorting 13 homolog A | Mõnikord (5–29%) | Esineb 1 haiguses |
| VPS35VPS35 retromer complex component | Mõnikord (5–29%) | Esineb 1 haiguses |
| XRCC2X-ray repair cross complementing 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CD28CD28 molecule | Harva (1–4%) | Esineb 1 haiguses |
| RB1RB transcriptional corepressor 1 | Harva (1–4%) | Esineb 1 haiguses |
| TNFRSF1BTNF receptor superfamily member 1B | Harva (1–4%) | Esineb 1 haiguses |
| CD244CD244 molecule | Pole registreeritud | Esineb 1 haiguses |
| CIITAclass II major histocompatibility complex transactivator | Pole registreeritud | Esineb 1 haiguses |
| CYP24A1cytochrome P450 family 24 subfamily A member 1 | Pole registreeritud | Esineb 1 haiguses |
| IL6interleukin 6 | Pole registreeritud | Esineb 1 haiguses |
| NFKBIL1NFKB inhibitor like 1 | Pole registreeritud | Esineb 1 haiguses |
| SLC22A4solute carrier family 22 member 4 | 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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