Tulajdonság
Hair loss
Klinikai név: Alopecia
A noncongenital process of hair loss, which may progress to partial or complete baldness.
Összefoglaló
- Szervrendszer
- Abnormality of the integument
Ez az oldal adatként
Adja hozzá a .json végződést az oldal címéhez, vagy kérjen application/json típust, hogy JSON-ként olvassa be.
library(jsonlite)
url <- "https://dantelabs.com/traits/alopecia.json"
page <- fromJSON(url)
page$trait$nameOlvassa el a(z) Hair loss nevű génhez kapcsolódó információkat, valamint a genomja többi részét egyetlen teszttel.
449 $-tólIngyenes szállítás · Eredmények 6–8 hét alatt
Kérem a Genome Testemet120 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.
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 18 of these genesGJA1MBTPS2DSPGJB3GJB4GJB6About this report →
- Hereditary Hypotrichosis, Woolly Hair and MonilethrixReads 12 of these genesKRT81KRT83LSSAPCDD1DSG4HRAbout this report →
- Inherited IchthyosesReads 13 of these genesCLDN1ABCA12ALOX12BALOXE3CERS3CYP4F22About this report →
- Ectodermal DysplasiasReads 11 of these genesKRT85NECTIN4EDAREDARADDGJB6IKBKGAbout this report →
Show 116 more reports
- Dyskeratosis CongenitaReads 12 of these genesACDCTC1DKC1NHP2NOP10NPM1About this report →
- Adams-Oliver SyndromeReads 6 of these genesDOCK6ARHGAP31DLL4EOGTNOTCH1RBPJAbout this report →
- Epidermolysis BullosaReads 9 of these genesPLECDSPKLHL24KRT14KRT5LAMA3About this report →
- Other Inborn Errors of ImmunityReads 27 of these genesDCLRE1CPOLD3RAG1RAG2ADAIL2RGAbout this report →
- Autoimmune DiseaseReads 8 of these genesKRASAIRECTLA4PRKCDTREX1FASAbout this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 4 of these genesKRASCTLA4PRKCDFASAbout this report →
- Severe Combined ImmunodeficiencyReads 8 of these genesDCLRE1CRAG1RAG2ADAIL2RGIL7RAbout this report →
- Acrodermatitis EnteropathicaReads 2 of these genesSLC30A2SLC39A4About this report →
- Biotinidase & Holocarboxylase DeficiencyReads 2 of these genesBTDHLCSAbout this report →
- Fibrodysplasia Ossificans ProgressivaReads 2 of these genesACVR1GNASAbout this report →
- Systemic Lupus ErythematosusReads 3 of these genesPRKCDTREX1SAT1About this report →
- DNA Repair DiseaseReads 8 of these genesDCLRE1CDDB2ERCC2ERCC3ERCC4ERCC5About this report →
- Immuno-Osseous DysplasiasReads 2 of these genesRMRPRNU4ATACAbout this report →
- Familial Pulmonary FibrosisReads 3 of these genesPARNRTEL1TERTAbout this report →
- Autoimmune Polyendocrine Syndrome Type 1 (APECED)Reads 1 of these genesAIREAbout this report →
- BAP1 Tumour Predisposition SyndromeReads 1 of these genesBAP1About this report →
- Björnstad SyndromeReads 1 of these genesBCS1LAbout this report →
- CHARGE SyndromeReads 1 of these genesCHD7About this report →
- CWC27-Related Retinitis Pigmentosa with Skeletal AnomaliesReads 1 of these genesCWC27About this report →
- Frontonasal Dysplasia with Alopecia and Genital Anomaly (ALX4)Reads 1 of these genesALX4About this report →
- GAPO SyndromeReads 1 of these genesANTXR1About this report →
- H SyndromeReads 1 of these genesSLC29A3About this report →
- IFAP Syndrome (MBTPS2)Reads 1 of these genesMBTPS2About this report →
- Johanson-Blizzard SyndromeReads 1 of these genesUBR1About this report →
- KDM1A-Related Neurodevelopmental DisorderReads 1 of these genesKDM1AAbout this report →
- Keutel SyndromeReads 1 of these genesMGPAbout this report →
- OFD1-Related CiliopathyReads 1 of these genesOFD1About this report →
- PIK3R1-Related DisordersReads 1 of these genesPIK3R1About this report →
- PLEC-Related Epidermolysis Bullosa and Muscular DystrophyReads 1 of these genesPLECAbout this report →
- PNPLA6-Related Ataxia, Retinal Dystrophy and HypogonadismReads 1 of these genesPNPLA6About this report →
- POLR3A-Related DisorderReads 1 of these genesPOLR3AAbout this report →
- Restrictive Dermopathy (ZMPSTE24)Reads 1 of these genesZMPSTE24About this report →
- Rett Syndrome and MECP2-Related DisordersReads 1 of these genesMECP2About this report →
- RNU4ATAC Spectrum DisorderReads 1 of these genesRNU4ATACAbout this report →
- Spondyloepiphyseal Dysplasia, Kondo-Fu TypeReads 1 of these genesMBTPS1About this report →
- X-Linked Adrenoleukodystrophy (ABCD1)Reads 1 of these genesABCD1About this report →
- X-linked Autoinflammatory DiseaseReads 1 of these genesIKBKGAbout this report →
- Common Variable Immunodeficiency (Monogenic CVID)Reads 3 of these genesCR2NFKB2NFKB1About this report →
- Hyper-IgE SyndromeReads 2 of these genesSPINK5ZNF341About this report →
- Inherited Parathyroid & Calcium-Sensing DisordersReads 2 of these genesCASRGNA11About this report →
- Inherited Predisposition to Acute Myeloid LeukaemiaReads 2 of these genesTERCTERTAbout this report →
- IPEX Syndrome and Other TregopathiesReads 2 of these genesCTLA4FOXP3About this report →
- Thyroid CancerReads 4 of these genesAIRECASRGNA11GNASAbout this report →
- Activated PI3K-Delta Syndrome (APDS)Reads 1 of these genesPIK3R1About this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 1 of these genesHTRA1About this report →
- Enlarged Parietal Foramina (MSX2)Reads 1 of these genesALX4About this report →
- PorphyriaReads 2 of these genesURODUROSAbout this report →
- Noonan SyndromeReads 3 of these genesHRASKRASNRASAbout this report →
- Agammaglobulinaemia (XLA and Autosomal Forms)Reads 2 of these genesPIK3R1BTKAbout this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 2 of these genesDCAF17FTLAbout this report →
- LipodystrophyReads 2 of these genesLMNAZMPSTE24About this report →
- Type I InterferonopathiesReads 2 of these genesPSMB10TREX1About this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7AAbout this report →
- Rothmund-Thomson SyndromeReads 1 of these genesRECQL4About this report →
- Van der Woude and Popliteal Pterygium Syndromes (IRF6)Reads 1 of these genesRIPK4About this report →
- Hypogonadotropic HypogonadismReads 4 of these genesDCAF17FGFR1RBM28CHD7About this report →
- Inherited Congenital Heart DefectsReads 2 of these genesFLNANOTCH1About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 3 of these genesPSMB10TNFAIP3TREX1About this report →
- Hypertrophic CardiomyopathyReads 4 of these genesHRASKRASNRASKLHL24About this report →
- Cutis LaxaReads 2 of these genesATP7ARIN2About this report →
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 1 of these genesARMC5About this report →
- Inherited Iron Metabolism DisordersReads 1 of these genesTMPRSS6About this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 1 of these genesGNASAbout this report →
- Amelogenesis ImperfectaReads 2 of these genesITGB6LAMB3About this report →
- Inherited Complement and Properdin DeficienciesReads 2 of these genesC4AC4BAbout this report →
- Inherited Neurodegenerative DisordersReads 9 of these genesATP7ADCAF17FTLPNPLA6POLR3ATREX1About this report →
- Other Inherited LeukodystrophiesReads 4 of these genesPOLR3ATREX1ABCD1PEX7About this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Ehlers-Danlos SyndromeReads 2 of these genesAEBP1COL3A1About this report →
- Hereditary Congenital & Juvenile CataractReads 2 of these genesLSSFTLAbout this report →
- Syndromic CraniosynostosisReads 2 of these genesFGFR1RECQL4About this report →
- Growth Hormone Insensitivity & IGF-1 Axis DisordersReads 1 of these genesSTAT5BAbout this report →
- HemochromatosisReads 1 of these genesHFEAbout this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Inflammatory Bowel Diseases (IBD)Reads 1 of these genesIL10About this report →
- VitreoretinopathyReads 2 of these genesIKBKGCTC1About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 2 of these genesERCC2ERCC5About this report →
- Classic Organic AciduriasReads 1 of these genesMCCC2About this report →
- Congenital Adrenal HyperplasiaReads 1 of these genesCYP11B1About this report →
- Hypodontia and AnodontiaReads 1 of these genesWNT10AAbout this report →
- Epilepsy (Full Panel)Reads 5 of these genesTMEM63BCSTBDMXL2FLNAMECP2About this report →
- Aicardi-Goutieres SyndromeReads 1 of these genesTREX1About this report →
- Hepatic Porphyria DisordersReads 1 of these genesURODAbout this report →
- Hereditary Rickets (Hypophosphatemic and Vitamin D-Dependent)Reads 1 of these genesVDRAbout this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Inherited ThrombocytopeniasReads 2 of these genesKDSRFLI1About this report →
- Limb-Girdle Muscular DystrophyReads 2 of these genesLMNAPLECAbout this report →
- Osteogenesis ImperfectaReads 2 of these genesMBTPS2POLR3AAbout this report →
- Kidney CancerReads 1 of these genesBAP1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 5 of these genesATP7ALMNABTDIARS2PEX7About this report →
- Congenital Disorders of GlycosylationReads 3 of these genesKRT5DOLKMOGSAbout this report →
- Arrhythmogenic CardiomyopathyReads 1 of these genesDSPAbout this report →
- Urinary and Renal System TumourReads 1 of these genesBAP1About this report →
- Dilated CardiomyopathyReads 2 of these genesLMNADOLKAbout this report →
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 1 of these genesPEX7About this report →
- Intellectual DisabilityReads 4 of these genesKDM6BSMARCA2MECP2NSDHLAbout this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 1 of these genesCYP11B1About this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 1 of these genesSOX18About this report →
- Hereditary Spastic ParaplegiaReads 2 of these genesPNPLA6ABCD1About this report →
- Fanconi AnemiaReads 1 of these genesERCC4About this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesATP7ALMNAAbout this report →
- Bardet-Biedl and Alström SyndromesReads 1 of these genesALMS1About this report →
- Hearing Loss and DeafnessReads 2 of these genesGJB6GJB2About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesPOLR3AAbout this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesRBM28About this report →
- Congenital Myasthenic SyndromeReads 1 of these genesPLECAbout this report →
- Spinal Muscular AtrophyReads 1 of these genesATP7AAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesSTUB1About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesDCAF17About this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesOFD1About this report →
- Female InfertilityReads 1 of these genesTP63About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesSTUB1About this report →
- Lysosomal Storage DiseaseReads 1 of these genesABHD5About this report →
- Leigh SyndromeReads 1 of these genesBTDAbout this report →
- Retinitis PigmentosaReads 1 of these genesOFD1About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesBCS1LAbout this report →
Olvassa el a(z) Hair loss nevű génhez kapcsolódó információkat, valamint a genomja többi részét egyetlen teszttel.
449 $-tólIngyenes szállítás · Eredmények 6–8 hét alatt
Kérem a Genome Testemet241 gén kapcsolódik ehhez: Hair loss
Ezeknek a géneknek a változásai olyan ritka betegségeket okoznak, amelyekben előfordul a(z) Hair loss. A tulajdonsággal rendelkező emberek többségének nincs ezek közül egyik betegsége sem, a listán szereplő gének pedig semmit nem mondanak el senki saját genomjáról.
| Gén | Milyen gyakran fordul elő | Betegségek |
|---|---|---|
| AHSGalpha 2-HS glycoprotein | Mindig | 2 betegségben |
| ANTXR1ANTXR cell adhesion molecule 1 | Mindig | 2 betegségben |
| ATP7AATPase copper transporting alpha | Mindig | 1 betegségben |
| BANF1barrier to autointegration nuclear assembly factor 1 | Mindig | 1 betegségben |
| BCS1LBCS1 ubiquinol-cytochrome c reductase complex chaperone | Mindig | 2 betegségben |
| CLDN1claudin 1 | Mindig | 1 betegségben |
| DCAF17DDB1 and CUL4 associated factor 17 | Mindig | 2 betegségben |
| DCLRE1CDNA cross-link repair 1C | Mindig | 2 betegségben |
| EDNRAendothelin receptor type A | Mindig | 1 betegségben |
| FAM111BFAM111 trypsin like peptidase B | Mindig | 1 betegségben |
| FGFR1fibroblast growth factor receptor 1 | Mindig | 2 betegségben |
| GJA1gap junction protein alpha 1 | Mindig | 2 betegségben |
| HEPHL1hephaestin like 1 | Mindig | 1 betegségben |
| KDM6Blysine demethylase 6B | Mindig | 1 betegségben |
| KRT81keratin 81 | Mindig | 1 betegségben |
| KRT83keratin 83 | Mindig | 1 betegségben |
| KRT85keratin 85 | Mindig | 1 betegségben |
| LSSlanosterol synthase | Mindig | 3 betegségben |
| MBTPS1membrane bound transcription factor peptidase, site 1 | Mindig | 1 betegségben |
| NECTIN4nectin cell adhesion molecule 4 | Mindig | 1 betegségben |
| PLD4phospholipase D family member 4 | Mindig | 1 betegségben |
| POLD3DNA polymerase delta 3, accessory subunit | Mindig | 1 betegségben |
| RAG1recombination activating 1 | Mindig | 2 betegségben |
| RAG2recombination activating 2 | Mindig | 2 betegségben |
| RBM28RNA binding motif protein 28 | Mindig | 2 betegségben |
| RIPK4receptor interacting serine/threonine kinase 4 | Mindig | 1 betegségben |
| RNU6ATACRNA, U6atac small nuclear | Mindig | 1 betegségben |
| SASH1SAM and SH3 domain containing 1 | Mindig | 1 betegségben |
| SLC30A2solute carrier family 30 member 2 | Mindig | 1 betegségben |
| SREBF1sterol regulatory element binding transcription factor 1 | Mindig | 1 betegségben |
| TM2D3TM2 domain containing 3 | Mindig | 1 betegségben |
| TMEM63Btransmembrane protein 63B | Mindig | 1 betegségben |
| TYMSthymidylate synthetase | Mindig | 2 betegségben |
| ZPR1ZPR1 zinc finger | Mindig | 1 betegségben |
| ADAadenosine deaminase | Nagyon gyakran (80–99%) | 1 betegségben |
| ALX4ALX homeobox 4 | Nagyon gyakran (80–99%) | 1 betegségben |
| APCDD1APC down-regulated 1 | Nagyon gyakran (80–99%) | 1 betegségben |
| CHD6chromodomain helicase DNA binding protein 6 | Nagyon gyakran (80–99%) | 1 betegségben |
| CHD7chromodomain helicase DNA binding protein 7 | Nagyon gyakran (80–99%) | 1 betegségben |
| DSG4desmoglein 4 | Nagyon gyakran (80–99%) | 1 betegségben |
További 201 gén megjelenítése
| Gén | Milyen gyakran fordul elő | Betegségek |
|---|---|---|
| EPS8L3EPS8 signaling adaptor L3 | Nagyon gyakran (80–99%) | 2 betegségben |
| FTLferritin light chain | Nagyon gyakran (80–99%) | 1 betegségben |
| HLA-DRAmajor histocompatibility complex, class II, DR alpha | Nagyon gyakran (80–99%) | 1 betegségben |
| HRHR lysine demethylase and nuclear receptor corepressor | Nagyon gyakran (80–99%) | 1 betegségben |
| HRASHRas proto-oncogene, GTPase | Nagyon gyakran (80–99%) | 2 betegségben |
| HTRA1HtrA serine peptidase 1 | Nagyon gyakran (80–99%) | 1 betegségben |
| IL2RGinterleukin 2 receptor subunit gamma | Nagyon gyakran (80–99%) | 1 betegségben |
| IL7Rinterleukin 7 receptor | Nagyon gyakran (80–99%) | 2 betegségben |
| ITGB6integrin subunit beta 6 | Nagyon gyakran (80–99%) | 1 betegségben |
| KRASKRas proto-oncogene, GTPase | Nagyon gyakran (80–99%) | 3 betegségben |
| LIPHlipase H | Nagyon gyakran (80–99%) | 1 betegségben |
| LMNAlamin A/C | Nagyon gyakran (80–99%) | 4 betegségben |
| LPAR6lysophosphatidic acid receptor 6 | Nagyon gyakran (80–99%) | 1 betegségben |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Nagyon gyakran (80–99%) | 4 betegségben |
| NRASNRAS proto-oncogene, GTPase | Nagyon gyakran (80–99%) | 2 betegségben |
| NUDCD3NudC domain containing 3 | Nagyon gyakran (80–99%) | 1 betegségben |
| PLECplectin | Nagyon gyakran (80–99%) | 1 betegségben |
| PSMB10proteasome 20S subunit beta 10 | Nagyon gyakran (80–99%) | 1 betegségben |
| RMRPRNA component of mitochondrial RNA processing endoribonuclease | Nagyon gyakran (80–99%) | 1 betegségben |
| RNU4ATACRNA, U4atac small nuclear | Nagyon gyakran (80–99%) | 1 betegségben |
| RPL21ribosomal protein L21 | Nagyon gyakran (80–99%) | 1 betegségben |
| SLC39A4solute carrier family 39 member 4 | Nagyon gyakran (80–99%) | 1 betegségben |
| SMARCA2SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 | Nagyon gyakran (80–99%) | 1 betegségben |
| SNRPEsmall nuclear ribonucleoprotein polypeptide E | Nagyon gyakran (80–99%) | 1 betegségben |
| SOX18SRY-box transcription factor 18 | Nagyon gyakran (80–99%) | 3 betegségben |
| UBR1ubiquitin protein ligase E3 component n-recognin 1 | Nagyon gyakran (80–99%) | 1 betegségben |
| ABCA12ATP binding cassette subfamily A member 12 | Gyakran (30–79%) | 2 betegségben |
| ABHD5abhydrolase domain containing 5, lysophosphatidic acid acyltransferase | Gyakran (30–79%) | 2 betegségben |
| ACVR1activin A receptor type 1 | Gyakran (30–79%) | 2 betegségben |
| AIREautoimmune regulator | Gyakran (30–79%) | 2 betegségben |
| ALOX12Barachidonate 12-lipoxygenase, 12R type | Gyakran (30–79%) | 3 betegségben |
| ALOXE3arachidonate epidermal lipoxygenase 3 | Gyakran (30–79%) | 3 betegségben |
| ASPRV1aspartic peptidase retroviral like 1 | Gyakran (30–79%) | 1 betegségben |
| BANK1B cell scaffold protein with ankyrin repeats 1 | Gyakran (30–79%) | 1 betegségben |
| BLKBLK proto-oncogene, Src family tyrosine kinase | Gyakran (30–79%) | 1 betegségben |
| BTDbiotinidase | Gyakran (30–79%) | 2 betegségben |
| C4Acomplement C4A (Chido/Rodgers blood group) | Gyakran (30–79%) | 1 betegségben |
| C4Bcomplement C4B (Chido/Rodgers blood group) | Gyakran (30–79%) | 1 betegségben |
| CASRcalcium sensing receptor | Gyakran (30–79%) | 1 betegségben |
| CD28CD28 molecule | Gyakran (30–79%) | 2 betegségben |
| CERS3ceramide synthase 3 | Gyakran (30–79%) | 1 betegségben |
| CR2complement C3d receptor 2 | Gyakran (30–79%) | 1 betegségben |
| CSTBcystatin B | Gyakran (30–79%) | 1 betegségben |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Gyakran (30–79%) | 3 betegségben |
| CYP4F22cytochrome P450 family 4 subfamily F member 22 | Gyakran (30–79%) | 1 betegségben |
| DMXL2Dmx like 2 | Gyakran (30–79%) | 1 betegségben |
| DNASE1deoxyribonuclease 1 | Gyakran (30–79%) | 2 betegségben |
| DOCK6dedicator of cytokinesis 6 | Gyakran (30–79%) | 2 betegségben |
| DSPdesmoplakin | Gyakran (30–79%) | 1 betegségben |
| EDARectodysplasin A receptor | Gyakran (30–79%) | 1 betegségben |
| EDARADDEDAR associated via death domain | Gyakran (30–79%) | 1 betegségben |
| ETS1ETS proto-oncogene 1, transcription factor | Gyakran (30–79%) | 1 betegségben |
| FCGR2AFc gamma receptor IIa | Gyakran (30–79%) | 1 betegségben |
| FCGR2BFc gamma receptor IIb | Gyakran (30–79%) | 2 betegségben |
| FCGR3BFc gamma receptor IIIb | Gyakran (30–79%) | 1 betegségben |
| FLNAfilamin A | Gyakran (30–79%) | 1 betegségben |
| GJB3gap junction protein beta 3 | Gyakran (30–79%) | 1 betegségben |
| GJB4gap junction protein beta 4 | Gyakran (30–79%) | 1 betegségben |
| GJB6gap junction protein beta 6 | Gyakran (30–79%) | 2 betegségben |
| GNA11G protein subunit alpha 11 | Gyakran (30–79%) | 1 betegségben |
| HLA-Bmajor histocompatibility complex, class I, B | Gyakran (30–79%) | 1 betegségben |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Gyakran (30–79%) | 4 betegségben |
| IGHG1immunoglobulin heavy constant gamma 1 (G1m marker) | Gyakran (30–79%) | 1 betegségben |
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | Gyakran (30–79%) | 2 betegségben |
| IL10interleukin 10 | Gyakran (30–79%) | 1 betegségben |
| IRAK1interleukin 1 receptor associated kinase 1 | Gyakran (30–79%) | 2 betegségben |
| IRF5interferon regulatory factor 5 | Gyakran (30–79%) | 1 betegségben |
| ITGAMintegrin subunit alpha M | Gyakran (30–79%) | 1 betegségben |
| JAZF1JAZF zinc finger 1 | Gyakran (30–79%) | 1 betegségben |
| KDSR3-ketodihydrosphingosine reductase | Gyakran (30–79%) | 1 betegségben |
| KIAA0319LKIAA0319 like | Gyakran (30–79%) | 1 betegségben |
| KLHL24kelch like family member 24 | Gyakran (30–79%) | 1 betegségben |
| KRT14keratin 14 | Gyakran (30–79%) | 2 betegségben |
| KRT5keratin 5 | Gyakran (30–79%) | 2 betegségben |
| LIPNlipase family member N | Gyakran (30–79%) | 1 betegségben |
| MANFmesencephalic astrocyte derived neurotrophic factor | Gyakran (30–79%) | 1 betegségben |
| MECP2methyl-CpG binding protein 2 | Gyakran (30–79%) | 1 betegségben |
| NECTIN1nectin cell adhesion molecule 1 | Gyakran (30–79%) | 1 betegségben |
| NFKB2nuclear factor kappa B subunit 2 | Gyakran (30–79%) | 1 betegségben |
| NIPAL4NIPA like domain containing 4 | Gyakran (30–79%) | 2 betegségben |
| OFD1OFD1 centriole and centriolar satellite protein | Gyakran (30–79%) | 2 betegségben |
| P4HA2prolyl 4-hydroxylase subunit alpha 2 | Gyakran (30–79%) | 1 betegségben |
| PDCD1programmed cell death 1 | Gyakran (30–79%) | 1 betegségben |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Gyakran (30–79%) | 1 betegségben |
| PNPLA1patatin like domain 1, omega-hydroxyceramide transacylase | Gyakran (30–79%) | 1 betegségben |
| PNPLA6patatin like domain 6, lysophospholipase | Gyakran (30–79%) | 2 betegségben |
| POLR3ARNA polymerase III subunit A | Gyakran (30–79%) | 1 betegségben |
| PRKCDprotein kinase C delta | Gyakran (30–79%) | 1 betegségben |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Gyakran (30–79%) | 3 betegségben |
| PXKPX domain containing serine/threonine kinase like | Gyakran (30–79%) | 1 betegségben |
| SDR9C7short chain dehydrogenase/reductase family 9C member 7 | Gyakran (30–79%) | 2 betegségben |
| SPINK5serine peptidase inhibitor Kazal type 5 | Gyakran (30–79%) | 1 betegségben |
| SPP1secreted phosphoprotein 1 | Gyakran (30–79%) | 2 betegségben |
| STAT4signal transducer and activator of transcription 4 | Gyakran (30–79%) | 2 betegségben |
| SULT2B1sulfotransferase family 2B member 1 | Gyakran (30–79%) | 2 betegségben |
| TGM1transglutaminase 1 | Gyakran (30–79%) | 4 betegségben |
| TLR7toll like receptor 7 | Gyakran (30–79%) | 2 betegségben |
| TNFAIP3TNF alpha induced protein 3 | Gyakran (30–79%) | 1 betegségben |
| TNFRSF1BTNF receptor superfamily member 1B | Gyakran (30–79%) | 2 betegségben |
| TNFSF4TNF superfamily member 4 | Gyakran (30–79%) | 1 betegségben |
| TNIP1TNFAIP3 interacting protein 1 | Gyakran (30–79%) | 1 betegségben |
| TP63tumor protein p63 | Gyakran (30–79%) | 2 betegségben |
| TREX1three prime repair exonuclease 1 | Gyakran (30–79%) | 2 betegségben |
| UBE2L3ubiquitin conjugating enzyme E2 L3 | Gyakran (30–79%) | 1 betegségben |
| VDRvitamin D receptor | Gyakran (30–79%) | 1 betegségben |
| WNT10AWnt family member 10A | Gyakran (30–79%) | 2 betegségben |
| ZMPSTE24zinc metallopeptidase STE24 | Gyakran (30–79%) | 2 betegségben |
| ACDACD shelterin complex subunit and telomerase recruitment factor | Néha (5–29%) | 1 betegségben |
| AEBP1AE binding protein 1 | Néha (5–29%) | 1 betegségben |
| ARHGAP31Rho GTPase activating protein 31 | Néha (5–29%) | 2 betegségben |
| ARMC5armadillo repeat containing 5 | Néha (5–29%) | 1 betegségben |
| BAP1BRCA1 associated deubiquitinase 1 | Néha (5–29%) | 1 betegségben |
| BTKBruton tyrosine kinase | Néha (5–29%) | 1 betegségben |
| BTNL2butyrophilin like 2 | Néha (5–29%) | 1 betegségben |
| COL3A1collagen type III alpha 1 chain | Néha (5–29%) | 1 betegségben |
| CRELD1CRELD disulfide isomerase 1 | Néha (5–29%) | 1 betegségben |
| CTC1CST telomere replication complex component 1 | Néha (5–29%) | 1 betegségben |
| CWC27CWC27 spliceosome associated cyclophilin | Néha (5–29%) | 2 betegségben |
| CYP11B1cytochrome P450 family 11 subfamily B member 1 | Néha (5–29%) | 1 betegségben |
| DDB2damage specific DNA binding protein 2 | Néha (5–29%) | 1 betegségben |
| DKC1dyskerin pseudouridine synthase 1 | Néha (5–29%) | 2 betegségben |
| DLL4delta like canonical Notch ligand 4 | Néha (5–29%) | 1 betegségben |
| DOLKdolichol kinase | Néha (5–29%) | 1 betegségben |
| DVL1dishevelled segment polarity protein 1 | Néha (5–29%) | 1 betegségben |
| DVL3dishevelled segment polarity protein 3 | Néha (5–29%) | 1 betegségben |
| EOGTEGF domain specific O-linked N-acetylglucosamine transferase | Néha (5–29%) | 1 betegségben |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | Néha (5–29%) | 1 betegségben |
| ERCC3ERCC excision repair 3, TFIIH core complex helicase subunit | Néha (5–29%) | 1 betegségben |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Néha (5–29%) | 1 betegségben |
| ERCC5ERCC excision repair 5, endonuclease | Néha (5–29%) | 1 betegségben |
| FASFas cell surface death receptor | Néha (5–29%) | 1 betegségben |
| FOXP3forkhead box P3 | Néha (5–29%) | 2 betegségben |
| FZD2frizzled class receptor 2 | Néha (5–29%) | 1 betegségben |
| GJB2gap junction protein beta 2 | Néha (5–29%) | 1 betegségben |
| GNASGNAS complex locus | Néha (5–29%) | 1 betegségben |
| H6PDhexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase | Néha (5–29%) | 1 betegségben |
| HLCSholocarboxylase synthetase | Néha (5–29%) | 2 betegségben |
| HRURFHR upstream open reading frame | Néha (5–29%) | 1 betegségben |
| IPO8importin 8 | Néha (5–29%) | 1 betegségben |
| KDM1Alysine demethylase 1A | Néha (5–29%) | 1 betegségben |
| LAMA3laminin subunit alpha 3 | Néha (5–29%) | 1 betegségben |
| LAMB3laminin subunit beta 3 | Néha (5–29%) | 1 betegségben |
| LAMC2laminin subunit gamma 2 | Néha (5–29%) | 1 betegségben |
| LEF1lymphoid enhancer binding factor 1 | Néha (5–29%) | 1 betegségben |
| LORICRINloricrin cornified envelope precursor protein | Néha (5–29%) | 1 betegségben |
| MGPmatrix Gla protein | Néha (5–29%) | 1 betegségben |
| MOGSmannosyl-oligosaccharide glucosidase | Néha (5–29%) | 1 betegségben |
| NFKB1nuclear factor kappa B subunit 1 | Néha (5–29%) | 1 betegségben |
| NHP2NHP2 ribonucleoprotein | Néha (5–29%) | 1 betegségben |
| NOP10NOP10 ribonucleoprotein | Néha (5–29%) | 1 betegségben |
| NOTCH1notch receptor 1 | Néha (5–29%) | 1 betegségben |
| NPM1nucleophosmin 1 | Néha (5–29%) | 1 betegségben |
| NSDHLNAD(P) dependent 3-beta-hydroxysteroid dehydrogenase NSDHL | Néha (5–29%) | 1 betegségben |
| NXNnucleoredoxin | Néha (5–29%) | 1 betegségben |
| ODC1ornithine decarboxylase 1 | Néha (5–29%) | 1 betegségben |
| PARNpoly(A)-specific ribonuclease | Néha (5–29%) | 2 betegségben |
| PERPp53 apoptosis effector related to PMP22 | Néha (5–29%) | 1 betegségben |
| RBPJrecombination signal binding protein for immunoglobulin kappa J region | Néha (5–29%) | 1 betegségben |
| ROR2ROR family WNT receptor 2 | Néha (5–29%) | 1 betegségben |
| RTEL1regulator of telomere elongation helicase 1 | Néha (5–29%) | 1 betegségben |
| SLC29A3solute carrier family 29 member 3 | Néha (5–29%) | 1 betegségben |
| STAT5Bsignal transducer and activator of transcription 5B | Néha (5–29%) | 1 betegségben |
| TERCtelomerase RNA component | Néha (5–29%) | 2 betegségben |
| TERTtelomerase reverse transcriptase | Néha (5–29%) | 2 betegségben |
| TINF2TERF1 interacting nuclear factor 2 | Néha (5–29%) | 3 betegségben |
| TRPV3transient receptor potential cation channel subfamily V member 3 | Néha (5–29%) | 1 betegségben |
| USB1U6 snRNA biogenesis phosphodiesterase 1 | Néha (5–29%) | 1 betegségben |
| WNT5AWnt family member 5A | Néha (5–29%) | 1 betegségben |
| WRAP53WD repeat containing antisense to TP53 | Néha (5–29%) | 1 betegségben |
| XPAXPA, DNA damage recognition and repair factor | Néha (5–29%) | 1 betegségben |
| XPCXPC complex subunit, DNA damage recognition and repair factor | Néha (5–29%) | 1 betegségben |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Ritkán (1–4%) | 1 betegségben |
| IARS2isoleucyl-tRNA synthetase 2, mitochondrial | Ritkán (1–4%) | 1 betegségben |
| KRT16keratin 16 | Ritkán (1–4%) | 1 betegségben |
| KRT17keratin 17 | Ritkán (1–4%) | 1 betegségben |
| KRT6Akeratin 6A | Ritkán (1–4%) | 1 betegségben |
| KRT6Bkeratin 6B | Ritkán (1–4%) | 1 betegségben |
| SAT1spermidine/spermine N1-acetyltransferase 1 | Ritkán (1–4%) | 1 betegségben |
| STUB1STIP1 homology and U-box containing protein 1 | Ritkán (1–4%) | 1 betegségben |
| TMPRSS6transmembrane serine protease 6 | Ritkán (1–4%) | 1 betegségben |
| ZNF341zinc finger protein 341 | Ritkán (1–4%) | 1 betegségben |
| ABCD1ATP binding cassette subfamily D member 1 | Nincs rögzítve | 1 betegségben |
| ALMS1ALMS1 centrosome and basal body associated protein | Nincs rögzítve | 1 betegségben |
| AP1B1adaptor related protein complex 1 subunit beta 1 | Nincs rögzítve | 1 betegségben |
| ATRATR checkpoint kinase | Nincs rögzítve | 1 betegségben |
| BMP2bone morphogenetic protein 2 | Nincs rögzítve | 1 betegségben |
| COL7A1collagen type VII alpha 1 chain | Nincs rögzítve | 1 betegségben |
| FOXN1forkhead box N1 | Nincs rögzítve | 1 betegségben |
| HFEhomeostatic iron regulator | Nincs rögzítve | 1 betegségben |
| HLA-DQA1major histocompatibility complex, class II, DQ alpha 1 | Nincs rögzítve | 1 betegségben |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Nincs rögzítve | 1 betegségben |
| KRT74keratin 74 | Nincs rögzítve | 1 betegségben |
| KRT86keratin 86 | Nincs rögzítve | 1 betegségben |
| MCCC2methylcrotonyl-CoA carboxylase subunit 2 | Nincs rögzítve | 1 betegségben |
| PEX7peroxisomal biogenesis factor 7 | Nincs rögzítve | 1 betegségben |
| PRKACAprotein kinase cAMP-activated catalytic subunit alpha | Nincs rögzítve | 1 betegségben |
| RECQL4RecQ like helicase 4 | Nincs rögzítve | 1 betegségben |
| RIN2Ras and Rab interactor 2 | Nincs rögzítve | 1 betegségben |
| SLITRK1SLIT and NTRK like family member 1 | Nincs rögzítve | 1 betegségben |
| URODuroporphyrinogen decarboxylase | Nincs rögzítve | 1 betegségben |
| UROSuroporphyrinogen III synthase | Nincs rögzítve | 1 betegségben |
Az, hogy milyen gyakran fordul elő a gén valamelyik állapotával élő emberek körében (a leggyakoribb érték, ahogyan a Human Phenotype Ontology rögzíti). Ezek az oldalak tulajdonságokat és az azok mögött álló kutatásokat ismertetik; nem diagnózist jelentenek. A tünetekkel kapcsolatban orvoshoz vagy genetikai tanácsadóhoz érdemes fordulni.
Szűkebb tulajdonságok
Tágabb tulajdonságok
Forrás
- Human Phenotype Ontology, 2026-09-01 kiadás: a tulajdonság, a nevei, a definíciója és a hozzá kapcsolt gének. További információ: hpo.jax.org.
- Adatkiadás: 2026.10.19-9814e911.
From traits to your genome
Read the genes behind these traits in your own DNA.
The Genome Test sequences nearly all of your DNA, not a preset panel, so every gene on these pages is in your data. Premium adds 810+ physician-ready reports.
Ingyenes szállítás · Eredmények 6–8 hét alatt
