AtlasKellele me abiks olemeMeie teadusTootedTulemused
Logi sisseKüsiSekveneeri oma genoom↗
Tunnus
Inguinal hernia
Protrusion of the contents of the abdominal cavity through the inguinal canal.
Kokkuvõte
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/inguinal-hernia.json"
page <- fromJSON(url)
page$trait$nameInguinal herniaHP:0000023
AtlasKellele me abiks olemeMeie teadusTootedTulemused
Logi sisseKüsiSekveneeri oma genoom↗
Lugege välja geenid, mis on seotud Inguinal hernia-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test152 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.
- Cutis LaxaReads 14 of these genesEFEMP1EFEMP2PYCR1ATP6V0A2ATP7AALDH18A1About this report →
- Aortic AneurysmReads 12 of these genesTGFBR1TGFBR2FBN1TGFB2ACTA2FOXE3About this report →
- Ehlers-Danlos SyndromeReads 14 of these genesCOL3A1DSEAEBP1COL1A1COL1A2COL5A1About this report →
- Intellectual DisabilityReads 41 of these genesBRD4KDM6BTAF4AP1S2CUL4BAHDC1About this report →
Show 148 more reports
- Marfan Like SyndromesReads 8 of these genesTGFBR1TGFBR2FBN1SKISMAD2SMAD3About this report →
- Loeys-Dietz SyndromeReads 6 of these genesTGFBR1TGFBR2SMAD2SMAD3TGFB2TGFB3About this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 6 of these genesNSD1CDKN1CH19HMGA2IGF2PLAG1About this report →
- Lysosomal Storage DiseaseReads 13 of these genesIDUAGUSBGNPTABGNSSGSHAGAAbout this report →
- Congenital Disorders of GlycosylationReads 15 of these genesDSEPIGWSLC37A4ATP6V0A2PIGLPIGYAbout this report →
- Syndromic Complex Neurodevelopmental DisorderReads 7 of these genesPAN2AP1S2ZFXBRPF1RNU4-2SETD5About this report →
- Coffin-Siris SyndromeReads 5 of these genesARID2ARID1ASMARCB1SMARCC2ARID1BAbout this report →
- FLNB-Related Skeletal Dysplasia (Larsen Spectrum)Reads 2 of these genesGZF1FLNBAbout this report →
- Inherited Congenital Heart DefectsReads 5 of these genesGATA4FLNAELNGATA6NOTCH1About this report →
- Osteogenesis ImperfectaReads 8 of these genesPYCR1SERPINH1ATP6V0A2COL1A1COL1A2MBTPS2About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 3 of these genesFLNAMYH11MYLKAbout this report →
- Joubert Syndrome And Related DisordersReads 7 of these genesTMEM107KIF7OFD1CC2D2AINPP5ERPGRIP1LAbout this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 5 of these genesGATA4AMHAMHR2HSD17B3ARAbout this report →
- Alpha-Mannosidosis and Other GlycoproteinosesReads 3 of these genesAGANEU1MAN2B1About this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 3 of these genesWDR19WDR35IFT122About this report →
- GPI Anchor Biosynthesis DefectsReads 5 of these genesPIGQPIGWPIGLPIGYPIGSAbout this report →
- Syndromic CraniosynostosisReads 5 of these genesWDR19WDR35IFT122SKIFGFR1About this report →
- Achondrogenesis panelReads 2 of these genesCOL2A1SLC26A2About this report →
- Mucopolysaccharidosis Type III (Sanfilippo Syndrome)Reads 2 of these genesGNSSGSHAbout this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 2 of these genesEZH2NSD1About this report →
- 22q11.2 Deletion SyndromeReads 1 of these genesTBX1About this report →
- Aarskog-Scott SyndromeReads 1 of these genesFGD1About this report →
- Androgen Insensitivity SyndromeReads 1 of these genesARAbout this report →
- ATP1A2-Related Fetal Akinesia with PolymicrogyriaReads 1 of these genesATP1A2About this report →
- BRAT1-Related Neurodevelopmental Disorder with Cerebellar AtrophyReads 1 of these genesBRAT1About this report →
- Burn-McKeown SyndromeReads 1 of these genesTXNL4AAbout this report →
- Caffey DiseaseReads 1 of these genesCOL1A1About this report →
- Catel-Manzke SyndromeReads 1 of these genesTGDSAbout this report →
- CHRNG-Related Multiple Pterygium SyndromeReads 1 of these genesCHRNGAbout this report →
- CWC27-Related Retinitis Pigmentosa with Skeletal AnomaliesReads 1 of these genesCWC27About this report →
- Dias-Logan SyndromeReads 1 of these genesBCL11AAbout this report →
- DICER1 Tumour PredispositionReads 1 of these genesDICER1About this report →
- DPH1-Related Developmental Delay with Short StatureReads 1 of these genesDPH1About this report →
- Dyssegmental Dysplasia, Silverman-Handmaker TypeReads 1 of these genesHSPG2About this report →
- FAT4-Related Neurodevelopmental DisorderReads 1 of these genesFAT4About this report →
- Ferguson-Smith Disease (Multiple Self-Healing Squamous Epithelioma)Reads 1 of these genesTGFBR1About this report →
- Floating-Harbor SyndromeReads 1 of these genesSRCAPAbout this report →
- Focal Dermal Hypoplasia (Goltz Syndrome)Reads 1 of these genesPORCNAbout this report →
- Frank-Ter Haar SyndromeReads 1 of these genesSH3PXD2BAbout this report →
- GM1 Gangliosidosis and Morquio B SyndromeReads 1 of these genesGLB1About this report →
- Greig Cephalopolysyndactyly SyndromeReads 1 of these genesGLI3About this report →
- Hajdu-Cheney SyndromeReads 1 of these genesNOTCH2About this report →
- IFAP Syndrome (MBTPS2)Reads 1 of these genesMBTPS2About this report →
- IFT140-Related CiliopathyReads 1 of these genesIFT140About this report →
- Mucopolysaccharidosis Type I (Hurler and Scheie Syndromes)Reads 1 of these genesIDUAAbout this report →
- Mucopolysaccharidosis Type II (Hunter Syndrome)Reads 1 of these genesIDSAbout this report →
- Mucopolysaccharidosis Type IVA (Morquio A Syndrome)Reads 1 of these genesGALNSAbout this report →
- Mucopolysaccharidosis Type VI (Maroteaux-Lamy Syndrome)Reads 1 of these genesARSBAbout this report →
- Mucopolysaccharidosis Type VII (Sly Syndrome)Reads 1 of these genesGUSBAbout this report →
- NFIA-Related Brain MalformationsReads 1 of these genesNFIAAbout this report →
- OFD1-Related CiliopathyReads 1 of these genesOFD1About this report →
- P5CS Deficiency (ALDH18A1-Related)Reads 1 of these genesALDH18A1About this report →
- Perlman SyndromeReads 1 of these genesDIS3L2About this report →
- PIK3R1-Related DisordersReads 1 of these genesPIK3R1About this report →
- PLD1-Related Congenital Heart DiseaseReads 1 of these genesPLD1About this report →
- POLR2A-Related Neurodevelopmental DisorderReads 1 of these genesPOLR2AAbout this report →
- Schwartz-Jampel Syndrome Type 1Reads 1 of these genesHSPG2About this report →
- Short-Rib Thoracic Dysplasia 7 (WDR35)Reads 1 of these genesWDR35About this report →
- Simpson-Golabi-Behmel SyndromeReads 1 of these genesGPC3About this report →
- SLC10A7-Related Skeletal Dysplasia With Amelogenesis ImperfectaReads 1 of these genesSLC10A7About this report →
- Snijders Blok-Campeau SyndromeReads 1 of these genesCHD3About this report →
- Spinal and Bulbar Muscular Atrophy (Kennedy Disease)Reads 1 of these genesARAbout this report →
- Spondyloepiphyseal Dysplasia With Congenital Joint DislocationsReads 1 of these genesCHST3About this report →
- Spondyloepiphyseal Dysplasia, Kondo-Fu TypeReads 1 of these genesMBTPS1About this report →
- Ulnar-Mammary SyndromeReads 1 of these genesTBX3About this report →
- UNC13A-Related Neurodevelopmental DisordersReads 1 of these genesUNC13AAbout this report →
- X-Linked Opitz G/BBB SyndromeReads 1 of these genesMID1About this report →
- Meckel SyndromeReads 3 of these genesTMEM107RPGRIP1LTMEM67About this report →
- Inherited ThrombocytopeniasReads 5 of these genesCDC42FLI1GP1BBRAP1BGNEAbout this report →
- Lissencephaly Spectrum DisordersReads 4 of these genesRAB3GAP2ARXPAFAH1B1APC2About this report →
- Cornelia de Lange SyndromeReads 2 of these genesBRD4NIPBLAbout this report →
- Epilepsy (Full Panel)Reads 11 of these genesDEPDC5PIGQFLNAATP1A2ATP6V1ARNF13About this report →
- Hypertrophic CardiomyopathyReads 6 of these genesNSD1CDKN1CH19IGF2MAPK1SHOC2About this report →
- Activated PI3K-Delta Syndrome (APDS)Reads 1 of these genesPIK3R1About this report →
- Alagille SyndromeReads 1 of these genesNOTCH2About this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 1 of these genesNOTCH3About this report →
- Dent Disease and Lowe SyndromeReads 1 of these genesOCRLAbout this report →
- Juvenile Polyposis SyndromeReads 1 of these genesSMAD4About this report →
- Lung CancerReads 1 of these genesDICER1About this report →
- Müllerian Aplasia (MRKH Syndrome)Reads 1 of these genesTBX6About this report →
- Otospondylomegaepiphyseal Dysplasia (OSMED)Reads 1 of these genesCOL2A1About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 3 of these genesWDR19NPHP3TMEM67About this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 2 of these genesCOL2A1SLC26A2About this report →
- Familial HypomagnesemiaReads 2 of these genesCLDN19TRPV6About this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7AAbout this report →
- Familial Hemiplegic MigraineReads 1 of these genesATP1A2About this report →
- Monogenic Precocious PubertyReads 1 of these genesDLK1About this report →
- Mucolipidoses (ML II, ML III and ML IV)Reads 1 of these genesGNPTABAbout this report →
- Rhabdoid Tumour and SWI/SNF Tumour PredispositionReads 1 of these genesSMARCB1About this report →
- Stargardt DiseaseReads 1 of these genesELOVL4About this report →
- Van der Woude and Popliteal Pterygium Syndromes (IRF6)Reads 1 of these genesRIPK4About this report →
- Inherited Neurodegenerative DisordersReads 11 of these genesATP7AALDH18A1ELOVL4NALCNSLC5A6CC2D2AAbout this report →
- Spinal Muscular AtrophyReads 3 of these genesATP7AEMILIN1UBA1About this report →
- Other Inborn Errors of ImmunityReads 8 of these genesPIK3R1DPP9NCF1RELTBX1SKIC2About this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 2 of these genesTUBBAPC2About this report →
- Primary Mitochondrial DiseaseReads 6 of these genesFBXL4NDUFA8DNAJC30MTFMTLRPPRCTMEM70About this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 2 of these genesFAT4MDFICAbout this report →
- Complex Neurodevelopmental Disorder (TRRAP, MYH10, RERE, SOX11)Reads 1 of these genesTRRAPAbout this report →
- Hereditary Hemorrhagic TelangiectasiaReads 1 of these genesSMAD4About this report →
- Molybdenum Cofactor & Isolated Sulfite Oxidase DeficiencyReads 1 of these genesGPHNAbout this report →
- Moyamoya DiseaseReads 1 of these genesACTA2About this report →
- NeurofibromatosisReads 1 of these genesSMARCB1About this report →
- TubulinopathiesReads 1 of these genesTUBBAbout this report →
- Ectodermal DysplasiasReads 2 of these genesHOXC13TP63About this report →
- Distal MyopathiesReads 2 of these genesDNAJB4GNEAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 7 of these genesFBXL4ATP7AFBLN5MTFMTSLC5A6EMILIN1About this report →
- Homocystinuria & Cobalamin DisordersReads 2 of these genesABCD4CBSAbout this report →
- Neonatal Diabetes MellitusReads 2 of these genesGATA4GATA6About this report →
- PancreatitisReads 1 of these genesTRPV6About this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Noonan SyndromeReads 2 of these genesMAPK1SHOC2About this report →
- Hypogonadotropic HypogonadismReads 3 of these genesSMCHD1RAB3GAP2FGFR1About this report →
- Adams-Oliver SyndromeReads 1 of these genesNOTCH1About this report →
- Chronic Granulomatous DiseaseReads 1 of these genesNCF1About this report →
- Peroxisomal Enzyme Disorders & Refsum DiseaseReads 1 of these genesGNPATAbout this report →
- Microphthalmia, Anophthalmia & ColobomaReads 2 of these genesRAB3GAP2STRA6About this report →
- Leigh SyndromeReads 3 of these genesFBXL4MTFMTLRPPRCAbout this report →
- Diabetes MellitusReads 2 of these genesGATA4GATA6About this report →
- Disorders of Glycine & Serine MetabolismReads 1 of these genesPHGDHAbout this report →
- GlaucomaReads 1 of these genesEFEMP1About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 2 of these genesSKIC2SKIC3About this report →
- Charcot-Marie-Tooth DiseaseReads 3 of these genesATP7AFBLN5EMILIN1About this report →
- Retinitis PigmentosaReads 3 of these genesIFT140OFD1CC2D2AAbout this report →
- Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome & AniridiaReads 1 of these genesFOXE3About this report →
- Inherited Platelet Function DisordersReads 1 of these genesGP1BBAbout this report →
- Agammaglobulinaemia (XLA and Autosomal Forms)Reads 1 of these genesPIK3R1About this report →
- Hereditary Macular DystrophiesReads 1 of these genesEFEMP1About this report →
- Heterotaxy & Laterality DefectsReads 1 of these genesGDF1About this report →
- Polycystic Kidney DiseaseReads 1 of these genesIFT140About this report →
- Severe Congenital NeutropeniaReads 1 of these genesG6PC3About this report →
- Methylmalonic & Propionic AcidemiaReads 1 of these genesABCD4About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 2 of these genesCC2D2ATMEM67About this report →
- Glycogen Storage DiseaseReads 1 of these genesSLC37A4About this report →
- Hereditary Spastic ParaplegiaReads 2 of these genesALDH18A1WASHC5About this report →
- Inherited Complement and Properdin DeficienciesReads 1 of these genesC1SAbout this report →
- Fanconi AnemiaReads 1 of these genesFANCBAbout this report →
- Hereditary Corneal DystrophiesReads 1 of these genesZEB1About this report →
- Autoimmune DiseaseReads 1 of these genesCHRNGAbout this report →
- Hereditary Congenital & Juvenile CataractReads 1 of these genesMAFAbout this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesGLI3About this report →
- VitreoretinopathyReads 1 of these genesCOL2A1About this report →
- Thyroid CancerReads 1 of these genesTRPV6About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesMBTPS2About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesELOVL4About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesTOR1AAbout this report →
- DNA Repair DiseaseReads 1 of these genesFANCBAbout this report →
- Male InfertilityReads 1 of these genesFKBP6About this report →
- Female InfertilityReads 1 of these genesTP63About this report →
Lugege välja geenid, mis on seotud Inguinal hernia-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test339 geeni on seotud tunnusega Inguinal hernia
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Inguinal hernia. 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 |
|---|---|---|
| ABCD4ATP binding cassette subfamily D member 4 | Alati | Esineb 1 haiguses |
| ARID2AT-rich interaction domain 2 | Alati | Esineb 1 haiguses |
| ATAD1ATPase family AAA domain containing 1 | Alati | Esineb 1 haiguses |
| BRD4bromodomain containing 4 | Alati | Esineb 1 haiguses |
| CACHD1cache domain containing 1 | Alati | Esineb 1 haiguses |
| CIROZciliated left-right organizer protein containing ZP-N domains | Alati | Esineb 1 haiguses |
| COL3A1collagen type III alpha 1 chain | Alati | Esineb 1 haiguses |
| DEPDC5DEP domain containing 5, GATOR1 subcomplex subunit | Alati | Esineb 1 haiguses |
| DHRS3dehydrogenase/reductase 3 | Alati | Esineb 1 haiguses |
| DMRT2doublesex and mab-3 related transcription factor 2 | Alati | Esineb 1 haiguses |
| DNAJB4DnaJ heat shock protein family (Hsp40) member B4 | Alati | Esineb 1 haiguses |
| DSEdermatan sulfate epimerase | Alati | Esineb 2 haiguses |
| EFEMP1EGF-like fibulin extracellular matrix protein 1 | Alati | Esineb 1 haiguses |
| EFEMP2EGF-like fibulin extracellular matrix protein 2 | Alati | Esineb 3 haiguses |
| ERI1exoribonuclease 1 | Alati | Esineb 1 haiguses |
| FARSBphenylalanyl-tRNA synthetase subunit beta | Alati | Esineb 1 haiguses |
| FAT4FAT atypical cadherin 4 | Alati | Esineb 1 haiguses |
| FBXL4F-box and leucine rich repeat protein 4 | Alati | Esineb 1 haiguses |
| FIBPFGF1 intracellular binding protein | Alati | Esineb 2 haiguses |
| GATA4GATA binding protein 4 | Alati | Esineb 1 haiguses |
| GNPATglyceronephosphate O-acyltransferase | Alati | Esineb 1 haiguses |
| IDUAalpha-L-iduronidase | Alati | Esineb 2 haiguses |
| KDM2Blysine demethylase 2B | Alati | Esineb 1 haiguses |
| KDM6Blysine demethylase 6B | Alati | Esineb 1 haiguses |
| MAN2B2mannosidase alpha class 2B member 2 | Alati | Esineb 1 haiguses |
| MBTPS1membrane bound transcription factor peptidase, site 1 | Alati | Esineb 1 haiguses |
| MED16mediator complex subunit 16 | Alati | Esineb 1 haiguses |
| NDUFA8NADH:ubiquinone oxidoreductase subunit A8 | Alati | Esineb 1 haiguses |
| PAN2poly(A) specific ribonuclease subunit PAN2 | Alati | Esineb 1 haiguses |
| PIGQphosphatidylinositol glycan anchor biosynthesis class Q | Alati | Esineb 1 haiguses |
| PIGWphosphatidylinositol glycan anchor biosynthesis class W | Alati | Esineb 1 haiguses |
| POLR1ARNA polymerase I subunit A | Alati | Esineb 1 haiguses |
| PYCR1pyrroline-5-carboxylate reductase 1 | Alati | Esineb 2 haiguses |
| SERPINH1serpin family H member 1 | Alati | Esineb 1 haiguses |
| SLC37A4solute carrier family 37 member 4 | Alati | Esineb 1 haiguses |
| SUPT7LSPT7 like, STAGA complex subunit gamma | Alati | Esineb 1 haiguses |
| TAF4TATA-box binding protein associated factor 4 | Alati | Esineb 1 haiguses |
| TGFBR1transforming growth factor beta receptor 1 | Alati | Esineb 2 haiguses |
| TGFBR2transforming growth factor beta receptor 2 | Alati | Esineb 2 haiguses |
| TMEM107transmembrane protein 107 | Alati | Esineb 1 haiguses |
Näita veel 299 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| TOR1Atorsin family 1 member A | Alati | Esineb 1 haiguses |
| UNC13Aunc-13 homolog A | Alati | Esineb 1 haiguses |
| WDR19WD repeat domain 19 | Alati | Esineb 1 haiguses |
| WDR35WD repeat domain 35 | Alati | Esineb 1 haiguses |
| AP1S2adaptor related protein complex 1 subunit sigma 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ATP6V0A2ATPase H+ transporting V0 subunit a2 | Väga sageli (80–99%) | Esineb 4 haiguses |
| ATP7AATPase copper transporting alpha | Väga sageli (80–99%) | Esineb 2 haiguses |
| CUL4Bcullin 4B | Väga sageli (80–99%) | Esineb 1 haiguses |
| FLNAfilamin A | Väga sageli (80–99%) | Esineb 1 haiguses |
| GUSBglucuronidase beta | Väga sageli (80–99%) | Esineb 1 haiguses |
| IRX5iroquois homeobox 5 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SMCHD1structural maintenance of chromosomes flexible hinge domain containing 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| ADAMTS15ADAM metallopeptidase with thrombospondin type 1 motif 15 | Sageli (30–79%) | Esineb 1 haiguses |
| AEBP1AE binding protein 1 | Sageli (30–79%) | Esineb 2 haiguses |
| AHDC1AT-hook DNA binding motif containing 1 | Sageli (30–79%) | Esineb 1 haiguses |
| ALDH18A1aldehyde dehydrogenase 18 family member A1 | Sageli (30–79%) | Esineb 2 haiguses |
| AMHanti-Mullerian hormone | Sageli (30–79%) | Esineb 2 haiguses |
| AMHR2anti-Mullerian hormone receptor type 2 | Sageli (30–79%) | Esineb 2 haiguses |
| ARID1AAT-rich interaction domain 1A | Sageli (30–79%) | Esineb 1 haiguses |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Sageli (30–79%) | Esineb 1 haiguses |
| ATP6V1AATPase H+ transporting V1 subunit A | Sageli (30–79%) | Esineb 2 haiguses |
| ATP6V1E1ATPase H+ transporting V1 subunit E1 | Sageli (30–79%) | Esineb 1 haiguses |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Sageli (30–79%) | Esineb 1 haiguses |
| BUB1BUB1 mitotic checkpoint serine/threonine kinase | Sageli (30–79%) | Esineb 1 haiguses |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Sageli (30–79%) | Esineb 1 haiguses |
| CLDN19claudin 19 | Sageli (30–79%) | Esineb 1 haiguses |
| CLIP2CAP-Gly domain containing linker protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| COL1A1collagen type I alpha 1 chain | Sageli (30–79%) | Esineb 3 haiguses |
| COL1A2collagen type I alpha 2 chain | Sageli (30–79%) | Esineb 3 haiguses |
| COX11cytochrome c oxidase copper chaperone COX11 | Sageli (30–79%) | Esineb 1 haiguses |
| DICER1dicer 1, ribonuclease III | Sageli (30–79%) | Esineb 1 haiguses |
| DLK1delta like non-canonical Notch ligand 1 | Sageli (30–79%) | Esineb 1 haiguses |
| DLX4distal-less homeobox 4 | Sageli (30–79%) | Esineb 1 haiguses |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Sageli (30–79%) | Esineb 1 haiguses |
| DPP9dipeptidyl peptidase 9 | Sageli (30–79%) | Esineb 1 haiguses |
| EIF4Heukaryotic translation initiation factor 4H | Sageli (30–79%) | Esineb 1 haiguses |
| ELNelastin | Sageli (30–79%) | Esineb 5 haiguses |
| ELOVL4ELOVL fatty acid elongase 4 | Sageli (30–79%) | Esineb 1 haiguses |
| EZH2enhancer of zeste 2 polycomb repressive complex 2 subunit | Sageli (30–79%) | Esineb 2 haiguses |
| FAAP100FA core complex associated protein 100 | Sageli (30–79%) | Esineb 1 haiguses |
| FBLN5fibulin 5 | Sageli (30–79%) | Esineb 3 haiguses |
| FBN1fibrillin 1 | Sageli (30–79%) | Esineb 2 haiguses |
| FEM1Bfem-1 homolog B | Sageli (30–79%) | Esineb 1 haiguses |
| FGD1FYVE, RhoGEF and PH domain containing 1 | Sageli (30–79%) | Esineb 2 haiguses |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Sageli (30–79%) | Esineb 1 haiguses |
| FOCADfocadhesin | Sageli (30–79%) | Esineb 1 haiguses |
| GDF11growth differentiation factor 11 | Sageli (30–79%) | Esineb 1 haiguses |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Sageli (30–79%) | Esineb 3 haiguses |
| GNSglucosamine (N-acetyl)-6-sulfatase | Sageli (30–79%) | Esineb 1 haiguses |
| GPC3glypican 3 | Sageli (30–79%) | Esineb 2 haiguses |
| GPC4glypican 4 | Sageli (30–79%) | Esineb 1 haiguses |
| GTF2Igeneral transcription factor IIi | Sageli (30–79%) | Esineb 1 haiguses |
| GTF2IRD1GTF2I repeat domain containing 1 | Sageli (30–79%) | Esineb 1 haiguses |
| GTF2IRD2GTF2I repeat domain containing 2 | Sageli (30–79%) | Esineb 1 haiguses |
| HOXC13homeobox C13 | Sageli (30–79%) | Esineb 1 haiguses |
| HSD17B3hydroxysteroid 17-beta dehydrogenase 3 | Sageli (30–79%) | Esineb 1 haiguses |
| IFT122intraflagellar transport 122 | Sageli (30–79%) | Esineb 1 haiguses |
| IFT140intraflagellar transport 140 | Sageli (30–79%) | Esineb 1 haiguses |
| IFT56intraflagellar transport 56 | Sageli (30–79%) | Esineb 1 haiguses |
| IPO8importin 8 | Sageli (30–79%) | Esineb 1 haiguses |
| ISL1ISL LIM homeobox 1 | Sageli (30–79%) | Esineb 1 haiguses |
| KDM5Blysine demethylase 5B | Sageli (30–79%) | Esineb 1 haiguses |
| KIF7kinesin family member 7 | Sageli (30–79%) | Esineb 3 haiguses |
| LIMK1LIM domain kinase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| LTBP1latent transforming growth factor beta binding protein 1 | Sageli (30–79%) | Esineb 2 haiguses |
| LTBP4latent transforming growth factor beta binding protein 4 | Sageli (30–79%) | Esineb 1 haiguses |
| MDFICMyoD family inhibitor domain containing | Sageli (30–79%) | Esineb 1 haiguses |
| MED12mediator complex subunit 12 | Sageli (30–79%) | Esineb 3 haiguses |
| MEG3maternally expressed 3 | Sageli (30–79%) | Esineb 1 haiguses |
| METTL27methyltransferase like 27 | Sageli (30–79%) | Esineb 1 haiguses |
| MTFMTmitochondrial methionyl-tRNA formyltransferase | Sageli (30–79%) | Esineb 1 haiguses |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Sageli (30–79%) | Esineb 2 haiguses |
| NALCNsodium leak channel, non-selective | Sageli (30–79%) | Esineb 1 haiguses |
| NCF1neutrophil cytosolic factor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NOTCH3notch receptor 3 | Sageli (30–79%) | Esineb 2 haiguses |
| NSD1nuclear receptor binding SET domain protein 1 | Sageli (30–79%) | Esineb 2 haiguses |
| OFD1OFD1 centriole and centriolar satellite protein | Sageli (30–79%) | Esineb 1 haiguses |
| PIEZO2piezo type mechanosensitive ion channel component 2 | Sageli (30–79%) | Esineb 2 haiguses |
| PIGLphosphatidylinositol glycan anchor biosynthesis class L | Sageli (30–79%) | Esineb 1 haiguses |
| PIGYphosphatidylinositol glycan anchor biosynthesis class Y | Sageli (30–79%) | Esineb 1 haiguses |
| PTDSS1phosphatidylserine synthase 1 | Sageli (30–79%) | Esineb 2 haiguses |
| RAB3GAP2RAB3 GTPase activating non-catalytic protein subunit 2 | Sageli (30–79%) | Esineb 1 haiguses |
| RFC2replication factor C subunit 2 | Sageli (30–79%) | Esineb 1 haiguses |
| RIPK4receptor interacting serine/threonine kinase 4 | Sageli (30–79%) | Esineb 1 haiguses |
| RNF13ring finger protein 13 | Sageli (30–79%) | Esineb 2 haiguses |
| RPL10ribosomal protein L10 | Sageli (30–79%) | Esineb 2 haiguses |
| RTL1retrotransposon Gag like 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SEC31ASEC31 homolog A, COPII component | Sageli (30–79%) | Esineb 1 haiguses |
| SGSHN-sulfoglucosamine sulfohydrolase | Sageli (30–79%) | Esineb 1 haiguses |
| SHPKsedoheptulokinase | Sageli (30–79%) | Esineb 1 haiguses |
| SKISKI proto-oncogene | Sageli (30–79%) | Esineb 2 haiguses |
| SLC10A7solute carrier family 10 member 7 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC2A10solute carrier family 2 member 10 | Sageli (30–79%) | Esineb 2 haiguses |
| SLC5A6solute carrier family 5 member 6 | Sageli (30–79%) | Esineb 1 haiguses |
| SMAD2SMAD family member 2 | Sageli (30–79%) | Esineb 2 haiguses |
| SMAD3SMAD family member 3 | Sageli (30–79%) | Esineb 3 haiguses |
| SMARCA2SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| SMARCB1SWI/SNF related BAF chromatin remodeling complex subunit B1 | Sageli (30–79%) | Esineb 1 haiguses |
| STX1Asyntaxin 1A | Sageli (30–79%) | Esineb 1 haiguses |
| SUZ12SUZ12 polycomb repressive complex 2 subunit | Sageli (30–79%) | Esineb 1 haiguses |
| TBL2transducin beta like 2 | Sageli (30–79%) | Esineb 1 haiguses |
| TGFB2transforming growth factor beta 2 | Sageli (30–79%) | Esineb 2 haiguses |
| TMEM270transmembrane protein 270 | Sageli (30–79%) | Esineb 1 haiguses |
| TP63tumor protein p63 | Sageli (30–79%) | Esineb 1 haiguses |
| VPS37DVPS37D subunit of ESCRT-I | Sageli (30–79%) | Esineb 1 haiguses |
| ZEB1zinc finger E-box binding homeobox 1 | Sageli (30–79%) | Esineb 1 haiguses |
| ZFXzinc finger protein X-linked | Sageli (30–79%) | Esineb 1 haiguses |
| ACTA2actin alpha 2, smooth muscle | Mõnikord (5–29%) | Esineb 1 haiguses |
| AGAaspartylglucosaminidase | Mõnikord (5–29%) | Esineb 1 haiguses |
| ARPC4actin related protein 2/3 complex subunit 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ARSBarylsulfatase B | Mõnikord (5–29%) | Esineb 1 haiguses |
| ARVCFARVCF delta catenin family member | Mõnikord (5–29%) | Esineb 1 haiguses |
| ARXaristaless related homeobox | Mõnikord (5–29%) | Esineb 1 haiguses |
| AUTS2activator of transcription and developmental regulator AUTS2 | Mõnikord (5–29%) | Esineb 2 haiguses |
| B3GAT3beta-1,3-glucuronyltransferase 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| B3GLCTbeta 3-glucosyltransferase | Mõnikord (5–29%) | Esineb 1 haiguses |
| BCL11ABCL11 transcription factor A | Mõnikord (5–29%) | Esineb 1 haiguses |
| BCRBCR activator of RhoGEF and GTPase | Mõnikord (5–29%) | Esineb 1 haiguses |
| BRF1BRF1 general transcription factor IIIB subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| BRPF1bromodomain and PHD finger containing 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CC2D2Acoiled-coil and C2 domain containing 2A | Mõnikord (5–29%) | Esineb 1 haiguses |
| CCDC22CCC complex scaffolding subunit CCDC22 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CDC42cell division cycle 42 | Mõnikord (5–29%) | Esineb 2 haiguses |
| CDKN1Ccyclin dependent kinase inhibitor 1C | Mõnikord (5–29%) | Esineb 1 haiguses |
| CHD3chromodomain helicase DNA binding protein 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CHRNGcholinergic receptor nicotinic gamma subunit | Mõnikord (5–29%) | Esineb 2 haiguses |
| CHST3carbohydrate sulfotransferase 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| COL5A1collagen type V alpha 1 chain | Mõnikord (5–29%) | Esineb 2 haiguses |
| COL5A2collagen type V alpha 2 chain | Mõnikord (5–29%) | Esineb 1 haiguses |
| COMTcatechol-O-methyltransferase | Mõnikord (5–29%) | Esineb 1 haiguses |
| CREBBPCREB binding lysine acetyltransferase | Mõnikord (5–29%) | Esineb 2 haiguses |
| CRELD1CRELD disulfide isomerase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CRKLCRK like proto-oncogene, adaptor protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| CSNK2A1casein kinase 2 alpha 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CTCFCCCTC-binding factor | Mõnikord (5–29%) | Esineb 1 haiguses |
| CTNND2catenin delta 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CWC27CWC27 spliceosome associated cyclophilin | Mõnikord (5–29%) | Esineb 1 haiguses |
| DGCR2DiGeorge syndrome critical region gene 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DGCR6DiGeorge syndrome critical region gene 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DGCR8DGCR8 microprocessor complex subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| DIS3L2DIS3 like 3'-5' exoribonuclease 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DLL3delta like canonical Notch ligand 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DPH1diphthamide biosynthesis 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DPH2diphthamide biosynthesis 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DPYSL5dihydropyrimidinase like 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DVL1dishevelled segment polarity protein 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| DVL3dishevelled segment polarity protein 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DYRK1Adual specificity tyrosine phosphorylation regulated kinase 1A | Mõnikord (5–29%) | Esineb 1 haiguses |
| EHMT1euchromatic histone lysine methyltransferase 1 | Mõnikord (5–29%) | Esineb 3 haiguses |
| EMILIN1elastin microfibril interfacer 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ESS2ess-2 spliceosome associated protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCBFA complementation group B | Mõnikord (5–29%) | Esineb 1 haiguses |
| FBXW11F-box and WD repeat domain containing 11 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FGFR1fibroblast growth factor receptor 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| FKBP14FKBP prolyl isomerase 14 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Mõnikord (5–29%) | Esineb 1 haiguses |
| FOXE3forkhead box E3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FZD2frizzled class receptor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| G6PC3glucose-6-phosphatase catalytic subunit 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GATA6GATA binding protein 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GDF1growth differentiation factor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GLI3GLI family zinc finger 3 | Mõnikord (5–29%) | Esineb 3 haiguses |
| GNB2G protein subunit beta 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GP1BBglycoprotein Ib platelet subunit beta | Mõnikord (5–29%) | Esineb 1 haiguses |
| GRIN2Bglutamate ionotropic receptor NMDA type subunit 2B | Mõnikord (5–29%) | Esineb 1 haiguses |
| GZF1GDNF inducible zinc finger protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| H19H19 imprinted maternally expressed transcript | Mõnikord (5–29%) | Esineb 1 haiguses |
| HES7hes family bHLH transcription factor 7 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HEY2hes related family bHLH transcription factor with YRPW motif 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HIRAhistone cell cycle regulator | Mõnikord (5–29%) | Esineb 1 haiguses |
| HMGA2high mobility group AT-hook 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HSPG2heparan sulfate proteoglycan 2 | Mõnikord (5–29%) | Esineb 2 haiguses |
| IGF2insulin like growth factor 2 | Mõnikord (5–29%) | Esineb 2 haiguses |
| INPP5Einositol polyphosphate-5-phosphatase E | Mõnikord (5–29%) | Esineb 1 haiguses |
| JMJD1Cjumonji domain containing 1C | Mõnikord (5–29%) | Esineb 1 haiguses |
| KCNQ1OT1KCNQ1 opposite strand/antisense transcript 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KDM3Blysine demethylase 3B | Mõnikord (5–29%) | Esineb 1 haiguses |
| KMT2Clysine methyltransferase 2C | Mõnikord (5–29%) | Esineb 1 haiguses |
| LFNGLFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase | Mõnikord (5–29%) | Esineb 1 haiguses |
| LOXlysyl oxidase | Mõnikord (5–29%) | Esineb 1 haiguses |
| LRPPRCleucine rich pentatricopeptide repeat containing | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAFMAF bZIP transcription factor | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAPK1mitogen-activated protein kinase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAPRE2microtubule associated protein RP/EB family member 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAT2Amethionine adenosyltransferase 2A | Mõnikord (5–29%) | Esineb 1 haiguses |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Mõnikord (5–29%) | Esineb 2 haiguses |
| MED25mediator complex subunit 25 | Mõnikord (5–29%) | Esineb 2 haiguses |
| MEIS2Meis homeobox 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MESP2mesoderm posterior bHLH transcription factor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MFAP5microfibril associated protein 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MID1midline 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| MLXIPLMLX interacting protein like | Mõnikord (5–29%) | Esineb 1 haiguses |
| MSL2MSL complex subunit 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MYH11myosin heavy chain 11 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MYH3myosin heavy chain 3 | Mõnikord (5–29%) | Esineb 3 haiguses |
| MYLKmyosin light chain kinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| NEU1neuraminidase 1 | Mõnikord (5–29%) | Esineb 3 haiguses |
| NIPBLNIPBL cohesin loading factor | Mõnikord (5–29%) | Esineb 1 haiguses |
| NOTCH1notch receptor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NOTCH2notch receptor 2 | Mõnikord (5–29%) | Esineb 2 haiguses |
| NPHP3nephrocystin 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NXNnucleoredoxin | Mõnikord (5–29%) | Esineb 1 haiguses |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Mõnikord (5–29%) | Esineb 1 haiguses |
| ODC1ornithine decarboxylase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| P3H1prolyl 3-hydroxylase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PACS1phosphofurin acidic cluster sorting protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PAFAH1B1platelet activating factor acetylhydrolase 1b regulatory subunit 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PHGDHphosphoglycerate dehydrogenase | Mõnikord (5–29%) | Esineb 1 haiguses |
| PIGSphosphatidylinositol glycan anchor biosynthesis class S | Mõnikord (5–29%) | Esineb 1 haiguses |
| PLAG1PLAG1 zinc finger | Mõnikord (5–29%) | Esineb 1 haiguses |
| PLOD1procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| POGZpogo transposable element derived with ZNF domain | Mõnikord (5–29%) | Esineb 2 haiguses |
| POLR2ARNA polymerase II subunit A | Mõnikord (5–29%) | Esineb 1 haiguses |
| PORCNporcupine O-acyltransferase | Mõnikord (5–29%) | Esineb 2 haiguses |
| PPP2CAprotein phosphatase 2 catalytic subunit alpha | Mõnikord (5–29%) | Esineb 1 haiguses |
| PPP2R1Aprotein phosphatase 2 scaffold subunit Aalpha | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRDM5PR/SET domain 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRKG1protein kinase cGMP-dependent 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PUF60poly(U) binding splicing factor 60 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RAP1BRAP1B, member of RAS oncogene family | Mõnikord (5–29%) | Esineb 1 haiguses |
| RELREL proto-oncogene, NF-kB subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| RIC1RIC1 partner of RAB6A GEF complex | Mõnikord (5–29%) | Esineb 1 haiguses |
| RIPPLY2ripply transcriptional repressor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RNU4-2RNA, U4 small nuclear 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ROR2ROR family WNT receptor 2 | Mõnikord (5–29%) | Esineb 2 haiguses |
| RPGRIP1LRPGRIP1 like | Mõnikord (5–29%) | Esineb 1 haiguses |
| RPL17ribosomal protein L17 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RPS6KA3ribosomal protein S6 kinase A3 | Mõnikord (5–29%) | Esineb 2 haiguses |
| RREB1ras responsive element binding protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SEC24CSEC24 homolog C, COPII component | Mõnikord (5–29%) | Esineb 1 haiguses |
| SEMA5Asemaphorin 5A | Mõnikord (5–29%) | Esineb 1 haiguses |
| SETSET nuclear proto-oncogene | Mõnikord (5–29%) | Esineb 1 haiguses |
| SETD5SET domain containing 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SH3PXD2BSH3 and PX domains 2B | Mõnikord (5–29%) | Esineb 1 haiguses |
| SHOC2SHOC2 leucine rich repeat scaffold protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| SMAD4SMAD family member 4 | Mõnikord (5–29%) | Esineb 2 haiguses |
| SMARCC2SWI/SNF related BAF chromatin remodeling complex subunit C2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SRCAPSnf2 related CREBBP activator protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| TASP1taspase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TBX1T-box transcription factor 1 | Mõnikord (5–29%) | Esineb 3 haiguses |
| TBX6T-box transcription factor 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TGFB3transforming growth factor beta 3 | Mõnikord (5–29%) | Esineb 2 haiguses |
| THSD4thrombospondin type 1 domain containing 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TMEM67transmembrane protein 67 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TNRC6Btrinucleotide repeat containing adaptor 6B | Mõnikord (5–29%) | Esineb 1 haiguses |
| TRAF7TNF receptor associated factor 7 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TRIM33tripartite motif containing 33 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TRPV6transient receptor potential cation channel subfamily V member 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TUBBtubulin beta class I | Mõnikord (5–29%) | Esineb 1 haiguses |
| TXNL4Athioredoxin like 4A | Mõnikord (5–29%) | Esineb 1 haiguses |
| UFD1ubiquitin recognition factor in ER associated degradation 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| VPS35LVPS35 endosomal protein sorting factor like | Mõnikord (5–29%) | Esineb 1 haiguses |
| WASHC5WASH complex subunit 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| WNT5AWnt family member 5A | Mõnikord (5–29%) | Esineb 2 haiguses |
| XPO1exportin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| YWHAEtyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon | Mõnikord (5–29%) | Esineb 1 haiguses |
| ADNPactivity dependent neuroprotector homeobox | Harva (1–4%) | Esineb 1 haiguses |
| APC2APC regulator of Wnt signaling pathway 2 | Harva (1–4%) | Esineb 1 haiguses |
| CHST14carbohydrate sulfotransferase 14 | Harva (1–4%) | Esineb 1 haiguses |
| CLCN4Cl-/H+ antiporter 4 | Harva (1–4%) | Esineb 1 haiguses |
| SETBP1SET binding protein 1 | Harva (1–4%) | Esineb 1 haiguses |
| SKIC2SKI2 subunit of superkiller complex | Harva (1–4%) | Esineb 1 haiguses |
| SKIC3SKI3 subunit of superkiller complex | Harva (1–4%) | Esineb 1 haiguses |
| TRRAPtransformation/transcription domain associated protein | Harva (1–4%) | Esineb 1 haiguses |
| ADAMTS2ADAM metallopeptidase with thrombospondin type 1 motif 2 | Pole registreeritud | Esineb 1 haiguses |
| ARandrogen receptor | Pole registreeritud | Esineb 1 haiguses |
| ARID1BAT-rich interaction domain 1B | Pole registreeritud | Esineb 1 haiguses |
| ASPNATaspartate N-acetyltransferase | Pole registreeritud | Esineb 1 haiguses |
| BMPERBMP binding endothelial regulator | Pole registreeritud | Esineb 1 haiguses |
| BRAT1BRCA1 associated ATM activator 1 | Pole registreeritud | Esineb 1 haiguses |
| C1Rcomplement C1r | Pole registreeritud | Esineb 1 haiguses |
| C1Scomplement C1s | Pole registreeritud | Esineb 1 haiguses |
| CBScystathionine beta-synthase | Pole registreeritud | Esineb 1 haiguses |
| COL2A1collagen type II alpha 1 chain | Pole registreeritud | Esineb 2 haiguses |
| DDX6DEAD-box helicase 6 | Pole registreeritud | Esineb 1 haiguses |
| FLNBfilamin B | Pole registreeritud | Esineb 1 haiguses |
| GALNSgalactosamine (N-acetyl)-6-sulfatase | Pole registreeritud | Esineb 1 haiguses |
| GLB1galactosidase beta 1 | Pole registreeritud | Esineb 2 haiguses |
| GLRA1glycine receptor alpha 1 | Pole registreeritud | Esineb 1 haiguses |
| GNEglucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | Pole registreeritud | Esineb 1 haiguses |
| GPHNgephyrin | Pole registreeritud | Esineb 1 haiguses |
| IDSiduronate 2-sulfatase | Pole registreeritud | Esineb 1 haiguses |
| LDHDlactate dehydrogenase D | Pole registreeritud | Esineb 1 haiguses |
| MAN2B1mannosidase alpha class 2B member 1 | Pole registreeritud | Esineb 1 haiguses |
| NFIAnuclear factor I A | Pole registreeritud | Esineb 1 haiguses |
| PLD1phospholipase D1 | Pole registreeritud | Esineb 1 haiguses |
| PLOD2procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 | Pole registreeritud | Esineb 1 haiguses |
| SATB2SATB homeobox 2 | Pole registreeritud | Esineb 1 haiguses |
| SIN3ASIN3 transcription regulator family member A | Pole registreeritud | Esineb 1 haiguses |
| SLC26A2solute carrier family 26 member 2 | Pole registreeritud | Esineb 1 haiguses |
| STRA6signaling receptor and transporter of retinol STRA6 | Pole registreeritud | Esineb 1 haiguses |
| TBX3T-box transcription factor 3 | Pole registreeritud | Esineb 1 haiguses |
| TGDSTDP-glucose 4,6-dehydratase | Pole registreeritud | Esineb 1 haiguses |
| TMCO1transmembrane and coiled-coil domains 1 | Pole registreeritud | Esineb 1 haiguses |
| TMEM70transmembrane protein 70 | Pole registreeritud | Esineb 1 haiguses |
| UBA1ubiquitin like modifier activating enzyme 1 | Pole registreeritud | Esineb 1 haiguses |
| WNK3WNK lysine deficient protein kinase 3 | Pole registreeritud | Esineb 1 haiguses |
| XRCC4X-ray repair cross complementing 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.
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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