AtlasVem vi hjälperVår vetenskapProdukterResultat
Logga inFrågaSekvensera ditt genom↗
Egenskap
Loss of bladder control
Kliniskt namn: Urinary incontinence
Loss of the ability to control the urinary bladder leading to involuntary urination.
Sammanfattning
- Även kallad
- Bladder incontinence
AtlasVem vi hjälperVår vetenskapProdukterResultat
Logga inFrågaSekvensera ditt genom↗
Den här sidan som data
Lägg till .json i sidans adress, eller begär application/json, för att läsa den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/urinary-incontinence.json"
page <- fromJSON(url)
page$trait$nameLoss of bladder controlHP:0000020
AtlasVem vi hjälperVår vetenskapProdukterResultat
Logga inFrågaSekvensera ditt genom↗
Läs generna kopplade till Loss of bladder control, och resten av ditt genom, med ett enda test.
Från 449 $Fri frakt · Resultat inom 6–8 veckor
Beställ mitt Genome Test92 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 Spastic ParaplegiaReads 26 of these genesRTN2ALDH18A1AP5Z1ATP13A2CPT1CCYP7B1About this report →
- Inherited Neurodegenerative DisordersReads 60 of these genesSLC44A1RTN2ALDH18A1ALS2AP5Z1ARSAAbout this report →
- Basal Ganglia CalcificationReads 7 of these genesPDGFBJAM2MYORGNAA60PDGFRBSLC20A2About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 11 of these genesALS2SQSTM1FUSSIGMAR1SPG11SPTLC1About this report →
Show 88 more reports
- Rare Hereditary Peripheral NeuropathiesReads 26 of these genesRTN2ARSANGFPSAPDNM2DNMT1About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 7 of these genesNGFDNMT1SPTLC1SPTLC2ATL1RETREG1About this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 2 of these genesHTRA1NOTCH3About this report →
- Metachromatic LeukodystrophyReads 2 of these genesARSAPSAPAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 8 of these genesATXN2KCND3STUB1CACNA1GDNMT1KCNC3About this report →
- Charcot-Marie-Tooth DiseaseReads 11 of these genesRTN2DNM2MORC2NEFLSBF1SIGMAR1About this report →
- Rhabdoid Tumour and SWI/SNF Tumour PredispositionReads 2 of these genesSMARCB1SMARCE1About this report →
- Other Inherited LeukodystrophiesReads 10 of these genesARSAGJC2HSPD1PSAPABCD1ALDH3A2About this report →
- Epilepsy (Full Panel)Reads 14 of these genesNEXMIFARXZEB2CHRNA2CHRNA4CHRNB2About this report →
- Adult-Onset Leukodystrophies (CSF1R, LMNB1, Nasu-Hakola)Reads 2 of these genesTREM2TYROBPAbout this report →
- NeurofibromatosisReads 2 of these genesNF2SMARCB1About this report →
- 3-Methylglutaconic Aciduria Type 1Reads 1 of these genesAUHAbout this report →
- 3-Methylglutaconic Aciduria Type 9 (TIMM50)Reads 1 of these genesTIMM50About this report →
- BAP1 Tumour Predisposition SyndromeReads 1 of these genesBAP1About this report →
- Christianson SyndromeReads 1 of these genesSLC9A6About this report →
- Curry-Jones Syndrome (Mosaic SMO Syndrome)Reads 1 of these genesSMOAbout this report →
- CYP7B1-Related Spastic Paraplegia and Liver DiseaseReads 1 of these genesCYP7B1About this report →
- DNMT1-Related Ataxia, Deafness and Narcolepsy (ADCA-DN)Reads 1 of these genesDNMT1About this report →
- FGFR3-Related Chondrodysplasias (Achondroplasia and Related Conditions)Reads 1 of these genesFGFR3About this report →
- Fragile X SyndromeReads 1 of these genesFMR1About this report →
- Gitelman SyndromeReads 1 of these genesSLC12A3About this report →
- KIF5A-Related Amyotrophic Lateral SclerosisReads 1 of these genesKIF5AAbout this report →
- Krabbe DiseaseReads 1 of these genesGALCAbout this report →
- Mowat-Wilson SyndromeReads 1 of these genesZEB2About this report →
- P5CS Deficiency (ALDH18A1-Related)Reads 1 of these genesALDH18A1About this report →
- Pompe DiseaseReads 1 of these genesGAAAbout this report →
- Siddiqi SyndromeReads 1 of these genesFITM2About this report →
- TRPV4-Related Skeletal DysplasiasReads 1 of these genesTRPV4About this report →
- X-Linked Adrenoleukodystrophy (ABCD1)Reads 1 of these genesABCD1About this report →
- Lysosomal Storage DiseaseReads 7 of these genesGAAAP5Z1ARSAPSAPGNEHEXBAbout this report →
- Frontotemporal DementiaReads 3 of these genesSQSTM1VCPCHMP2BAbout this report →
- Cowden Syndrome (PTEN hamartoma tumour syndrome)Reads 1 of these genesAKT1About this report →
- Hereditary FibromatosesReads 1 of these genesPDGFRBAbout this report →
- Malignant Hyperthermia SusceptibilityReads 1 of these genesRYR1About this report →
- Nevoid Basal Cell Carcinoma (Gorlin) SyndromeReads 1 of these genesSUFUAbout this report →
- Sandhoff Disease and GM2 Activator DeficiencyReads 1 of these genesHEXBAbout this report →
- Congenital MyopathiesReads 3 of these genesBIN1DNM2RYR1About this report →
- Familial Pulmonary FibrosisReads 2 of these genesPOT1TERTAbout this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 2 of these genesATP13A2PANK2About this report →
- Coffin-Siris SyndromeReads 2 of these genesSMARCB1SMARCE1About this report →
- Hereditary AmyloidosisReads 2 of these genesCST3TTRAbout this report →
- Cerebral Amyloid AngiopathyReads 1 of these genesCST3About this report →
- MedulloblastomaReads 1 of these genesSUFUAbout this report →
- Myofibrillar MyopathiesReads 2 of these genesKYRYR1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 4 of these genesSACSSTUB1SYNE1FLVCR1About this report →
- Parkinson DiseaseReads 2 of these genesATP13A2VPS13CAbout this report →
- Familial Paget Disease of BoneReads 1 of these genesSQSTM1About this report →
- MelanomaReads 1 of these genesPOT1About this report →
- Distal MyopathiesReads 2 of these genesGNEVCPAbout this report →
- Intellectual DisabilityReads 7 of these genesNEXMIFRSRC1ADNPZEB2TRIOSMARCB1About this report →
- Alzheimer diseaseReads 1 of these genesTREM2About this report →
- Bartter DiseaseReads 1 of these genesCLCNKBAbout this report →
- MTOR Pathway Megalencephaly and Overgrowth DisordersReads 1 of these genesPIK3CAAbout this report →
- Dyskeratosis CongenitaReads 2 of these genesPOT1TERTAbout this report →
- Syndromic Complex Neurodevelopmental DisorderReads 2 of these genesZMYM2TRAF7About this report →
- Syndromic CraniosynostosisReads 2 of these genesFGFR3SMOAbout this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 2 of these genesGJC2HSPD1About this report →
- Spinal Muscular AtrophyReads 2 of these genesSIGMAR1IGHMBP2About this report →
- Inherited Predisposition to Acute Myeloid LeukaemiaReads 1 of these genesTERTAbout this report →
- Disorders of Glycine & Serine MetabolismReads 1 of these genesSLC1A4About this report →
- Hepatic Porphyria DisordersReads 1 of these genesHMBSAbout this report →
- Complex Neurodevelopmental Disorder With Motor FeaturesReads 1 of these genesKMT2BAbout this report →
- Kidney CancerReads 1 of these genesBAP1About this report →
- PorphyriaReads 1 of these genesHMBSAbout this report →
- Congenital Disorders of GlycosylationReads 3 of these genesCOG5GNEGALNT2About this report →
- Hermansky-Pudlak SyndromeReads 1 of these genesHPS6About this report →
- Urinary and Renal System TumourReads 1 of these genesBAP1About this report →
- Neuronal Ceroid LipofuscinosisReads 1 of these genesATP13A2About this report →
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 1 of these genesPEX11BAbout this report →
- Glycogen Storage DiseaseReads 1 of these genesGBE1About this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 1 of these genesCACNA1HAbout this report →
- Cutis LaxaReads 1 of these genesALDH18A1About this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 1 of these genesGJC2About this report →
- Congenital Stationary Night BlindnessReads 1 of these genesCABP4About this report →
- Neonatal Diabetes MellitusReads 1 of these genesMNX1About this report →
- Bardet-Biedl and Alström SyndromesReads 1 of these genesALMS1About this report →
- Lissencephaly Spectrum DisordersReads 1 of these genesARXAbout this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesSMOAbout this report →
- Diabetes MellitusReads 1 of these genesMNX1About this report →
- Inherited ThrombocytopeniasReads 1 of these genesGNEAbout this report →
- Primary Mitochondrial DiseaseReads 2 of these genesFARS2COQ2About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesKMT2BAbout this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesSUFUAbout this report →
- Male InfertilityReads 1 of these genesCFAP43About this report →
- Dilated CardiomyopathyReads 1 of these genesSYNE1About this report →
- Female InfertilityReads 1 of these genesFMR1About this report →
- Leigh SyndromeReads 1 of these genesFARS2About this report →
- Retinitis PigmentosaReads 1 of these genesFLVCR1About this report →
Läs generna kopplade till Loss of bladder control, och resten av ditt genom, med ett enda test.
Från 449 $Fri frakt · Resultat inom 6–8 veckor
Beställ mitt Genome Test165 gener kopplade till Loss of bladder control
Förändringar i dessa gener orsakar sällsynta tillstånd där Loss of bladder control förekommer. De flesta med denna egenskap har inget av dessa tillstånd, och en gen på listan säger ingenting om någons eget genom.
| Gen | Hur ofta den förekommer | Tillstånd |
|---|---|---|
| BORCS8BLOC-1 related complex subunit 8 | Alltid | I 1 tillstånd |
| CST3cystatin C | Alltid | I 1 tillstånd |
| FRYLFRY like transcription coactivator | Alltid | I 1 tillstånd |
| GAAalpha glucosidase | Alltid | I 1 tillstånd |
| GBE11,4-alpha-glucan branching enzyme 1 | Alltid | I 2 tillstånd |
| GGT1gamma-glutamyltransferase 1 | Alltid | I 1 tillstånd |
| HS6ST2heparan sulfate 6-O-sulfotransferase 2 | Alltid | I 1 tillstånd |
| HTRA1HtrA serine peptidase 1 | Alltid | I 1 tillstånd |
| KMT2Blysine methyltransferase 2B | Alltid | I 1 tillstånd |
| KYkyphoscoliosis peptidase | Alltid | I 1 tillstånd |
| NEXMIFneurite extension and migration factor | Alltid | I 1 tillstånd |
| NOTCH3notch receptor 3 | Alltid | I 2 tillstånd |
| POT1protection of telomeres 1 | Alltid | I 1 tillstånd |
| RSRC1arginine and serine rich coiled-coil 1 | Alltid | I 1 tillstånd |
| SLC44A1solute carrier family 44 member 1 | Alltid | I 1 tillstånd |
| TOP2BDNA topoisomerase II beta | Alltid | I 1 tillstånd |
| ADNPactivity dependent neuroprotector homeobox | Mycket ofta (80–99 %) | I 1 tillstånd |
| RTN2reticulon 2 | Mycket ofta (80–99 %) | I 2 tillstånd |
| ACBD6acyl-CoA binding domain containing 6 | Ofta (30–79 %) | I 1 tillstånd |
| ALDH18A1aldehyde dehydrogenase 18 family member A1 | Ofta (30–79 %) | I 3 tillstånd |
| ALS2alsin Rho guanine nucleotide exchange factor ALS2 | Ofta (30–79 %) | I 3 tillstånd |
| AP5Z1adaptor related protein complex 5 subunit zeta 1 | Ofta (30–79 %) | I 2 tillstånd |
| ARSAarylsulfatase A | Ofta (30–79 %) | I 4 tillstånd |
| ARXaristaless related homeobox | Ofta (30–79 %) | I 1 tillstånd |
| ATP13A2ATPase cation transporting 13A2 | Ofta (30–79 %) | I 2 tillstånd |
| ATXN2ataxin 2 | Ofta (30–79 %) | I 1 tillstånd |
| COPB1coat protein complex I subunit beta 1 | Ofta (30–79 %) | I 1 tillstånd |
| CPT1Ccarnitine palmitoyltransferase 1C | Ofta (30–79 %) | I 1 tillstånd |
| CYP7B1cytochrome P450 family 7 subfamily B member 1 | Ofta (30–79 %) | I 1 tillstånd |
| DDHD2DDHD domain containing 2 | Ofta (30–79 %) | I 1 tillstånd |
| DPH5diphthamide biosynthesis 5 | Ofta (30–79 %) | I 1 tillstånd |
| GJC2gap junction protein gamma 2 | Ofta (30–79 %) | I 1 tillstånd |
| HPSE2heparanase 2 (inactive) | Ofta (30–79 %) | I 1 tillstånd |
| HSPD1heat shock protein family D (Hsp60) member 1 | Ofta (30–79 %) | I 2 tillstånd |
| KCND3potassium voltage-gated channel subfamily D member 3 | Ofta (30–79 %) | I 1 tillstånd |
| LRIG2leucine rich repeats and immunoglobulin like domains 2 | Ofta (30–79 %) | I 1 tillstånd |
| MYO1Hmyosin IH | Ofta (30–79 %) | I 1 tillstånd |
| NGFnerve growth factor | Ofta (30–79 %) | I 1 tillstånd |
| NOTCH2NLCnotch 2 N-terminal like C | Ofta (30–79 %) | I 1 tillstånd |
| PPFIA3PPFI scaffold protein A3 | Ofta (30–79 %) | I 1 tillstånd |
Visa 125 gener till
| Gen | Hur ofta den förekommer | Tillstånd |
|---|---|---|
| PSAPprosaposin | Ofta (30–79 %) | I 4 tillstånd |
| SACSsacsin molecular chaperone | Ofta (30–79 %) | I 1 tillstånd |
| SPG7SPG7 matrix AAA peptidase subunit, paraplegin | Ofta (30–79 %) | I 1 tillstånd |
| SQSTM1sequestosome 1 | Ofta (30–79 %) | I 1 tillstånd |
| STUB1STIP1 homology and U-box containing protein 1 | Ofta (30–79 %) | I 1 tillstånd |
| UBAP1ubiquitin associated protein 1 | Ofta (30–79 %) | I 1 tillstånd |
| VPS13Cvacuolar protein sorting 13 homolog C | Ofta (30–79 %) | I 1 tillstånd |
| WASHC5WASH complex subunit 5 | Ofta (30–79 %) | I 2 tillstånd |
| ZEB2zinc finger E-box binding homeobox 2 | Ofta (30–79 %) | I 2 tillstånd |
| ABCD1ATP binding cassette subfamily D member 1 | Ibland (5–29 %) | I 2 tillstånd |
| ALMS1ALMS1 centrosome and basal body associated protein | Ibland (5–29 %) | I 1 tillstånd |
| ATXN8ataxin 8 | Ibland (5–29 %) | I 1 tillstånd |
| ATXN8OSATXN8 opposite strand lncRNA | Ibland (5–29 %) | I 1 tillstånd |
| BIN1bridging integrator 1 | Ibland (5–29 %) | I 1 tillstånd |
| BNC2basonuclin zinc finger protein 2 | Ibland (5–29 %) | I 2 tillstånd |
| CABP4calcium binding protein 4 | Ibland (5–29 %) | I 1 tillstånd |
| CACNA1Gcalcium voltage-gated channel subunit alpha1 G | Ibland (5–29 %) | I 2 tillstånd |
| CAPN1calpain 1 | Ibland (5–29 %) | I 1 tillstånd |
| CHRNA2cholinergic receptor nicotinic alpha 2 subunit | Ibland (5–29 %) | I 1 tillstånd |
| CHRNA4cholinergic receptor nicotinic alpha 4 subunit | Ibland (5–29 %) | I 1 tillstånd |
| CHRNB2cholinergic receptor nicotinic beta 2 subunit | Ibland (5–29 %) | I 1 tillstånd |
| COG5component of oligomeric golgi complex 5 | Ibland (5–29 %) | I 1 tillstånd |
| CRHcorticotropin releasing hormone | Ibland (5–29 %) | I 1 tillstånd |
| DEPDC5DEP domain containing 5, GATOR1 subcomplex subunit | Ibland (5–29 %) | I 1 tillstånd |
| DKK1dickkopf Wnt signaling pathway inhibitor 1 | Ibland (5–29 %) | I 1 tillstånd |
| DNM2dynamin 2 | Ibland (5–29 %) | I 1 tillstånd |
| DNMT1DNA methyltransferase 1 | Ibland (5–29 %) | I 1 tillstånd |
| EIF2AK2eukaryotic translation initiation factor 2 alpha kinase 2 | Ibland (5–29 %) | I 1 tillstånd |
| ERLIN1ER lipid raft associated 1 | Ibland (5–29 %) | I 1 tillstånd |
| FA2Hfatty acid 2-hydroxylase | Ibland (5–29 %) | I 2 tillstånd |
| FARS2phenylalanyl-tRNA synthetase 2, mitochondrial | Ibland (5–29 %) | I 1 tillstånd |
| FGFR3fibroblast growth factor receptor 3 | Ibland (5–29 %) | I 1 tillstånd |
| FITM2fat storage inducing transmembrane protein 2 | Ibland (5–29 %) | I 1 tillstånd |
| FRMD5FERM domain containing 5 | Ibland (5–29 %) | I 1 tillstånd |
| FUSFUS RNA binding protein | Ibland (5–29 %) | I 1 tillstånd |
| GBA2glucosylceramidase beta 2 | Ibland (5–29 %) | I 3 tillstånd |
| GNEglucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | Ibland (5–29 %) | I 1 tillstånd |
| HACE1HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 | Ibland (5–29 %) | I 1 tillstånd |
| HEXBhexosaminidase subunit beta | Ibland (5–29 %) | I 2 tillstånd |
| HPS6HPS6 biogenesis of lysosomal organelles complex 2 subunit 3 | Ibland (5–29 %) | I 1 tillstånd |
| KCNC3potassium voltage-gated channel subfamily C member 3 | Ibland (5–29 %) | I 1 tillstånd |
| KCNT1potassium sodium-activated channel subfamily T member 1 | Ibland (5–29 %) | I 1 tillstånd |
| MORC2MORC family CW-type zinc finger 2 | Ibland (5–29 %) | I 2 tillstånd |
| MTMR14myotubularin related protein 14 | Ibland (5–29 %) | I 1 tillstånd |
| MYF6myogenic factor 6 | Ibland (5–29 %) | I 1 tillstånd |
| NEFLneurofilament light chain | Ibland (5–29 %) | I 1 tillstånd |
| NIPA1NIPA magnesium transporter 1 | Ibland (5–29 %) | I 2 tillstånd |
| RNF170ring finger protein 170 | Ibland (5–29 %) | I 1 tillstånd |
| RYR1ryanodine receptor 1 | Ibland (5–29 %) | I 1 tillstånd |
| SBF1SET binding factor 1 | Ibland (5–29 %) | I 1 tillstånd |
| SIGMAR1sigma receptor chaperone 1 | Ibland (5–29 %) | I 1 tillstånd |
| SLC1A4solute carrier family 1 member 4 | Ibland (5–29 %) | I 1 tillstånd |
| SORDsorbitol dehydrogenase | Ibland (5–29 %) | I 1 tillstånd |
| SPG11SPG11 vesicle trafficking associated, spatacsin | Ibland (5–29 %) | I 3 tillstånd |
| SPTLC1serine palmitoyltransferase long chain base subunit 1 | Ibland (5–29 %) | I 1 tillstånd |
| SPTLC2serine palmitoyltransferase long chain base subunit 2 | Ibland (5–29 %) | I 1 tillstånd |
| SYNE1spectrin repeat containing nuclear envelope protein 1 | Ibland (5–29 %) | I 2 tillstånd |
| TARDBPTAR DNA binding protein | Ibland (5–29 %) | I 1 tillstånd |
| TBCDtubulin folding cofactor D | Ibland (5–29 %) | I 2 tillstånd |
| TIMM50translocase of inner mitochondrial membrane 50 | Ibland (5–29 %) | I 2 tillstånd |
| TRIOtrio Rho guanine nucleotide exchange factor | Ibland (5–29 %) | I 1 tillstånd |
| TRMT2BtRNA methyltransferase 2B | Ibland (5–29 %) | I 1 tillstånd |
| UBQLN2ubiquilin 2 | Ibland (5–29 %) | I 1 tillstånd |
| VCPvalosin containing protein | Ibland (5–29 %) | I 1 tillstånd |
| ZMYM2zinc finger MYM-type containing 2 | Ibland (5–29 %) | I 1 tillstånd |
| AKT1AKT serine/threonine kinase 1 | Sällan (1–4%) | I 1 tillstånd |
| ALDH3A2aldehyde dehydrogenase 3 family member A2 | Sällan (1–4%) | I 1 tillstånd |
| BAP1BRCA1 associated deubiquitinase 1 | Sällan (1–4%) | I 1 tillstånd |
| CACNA1Hcalcium voltage-gated channel subunit alpha1 H | Sällan (1–4%) | I 1 tillstånd |
| CLCNKBchloride voltage-gated channel Kb | Sällan (1–4%) | I 1 tillstånd |
| GABRA1gamma-aminobutyric acid type A receptor subunit alpha1 | Sällan (1–4%) | I 1 tillstånd |
| GABRB3gamma-aminobutyric acid type A receptor subunit beta3 | Sällan (1–4%) | I 1 tillstånd |
| GABRG2gamma-aminobutyric acid type A receptor subunit gamma2 | Sällan (1–4%) | I 1 tillstånd |
| GALCgalactosylceramidase | Sällan (1–4%) | I 1 tillstånd |
| HMBShydroxymethylbilane synthase | Sällan (1–4%) | I 2 tillstånd |
| JRKJrk helix-turn-helix protein | Sällan (1–4%) | I 1 tillstånd |
| NF2NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor | Sällan (1–4%) | I 1 tillstånd |
| PDGFBplatelet derived growth factor subunit B | Sällan (1–4%) | I 2 tillstånd |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Sällan (1–4%) | I 1 tillstånd |
| SLC12A3solute carrier family 12 member 3 | Sällan (1–4%) | I 1 tillstånd |
| SMARCB1SWI/SNF related BAF chromatin remodeling complex subunit B1 | Sällan (1–4%) | I 1 tillstånd |
| SMARCE1SWI/SNF related BAF chromatin remodeling complex subunit E1 | Sällan (1–4%) | I 1 tillstånd |
| SMOsmoothened, frizzled class receptor | Sällan (1–4%) | I 1 tillstånd |
| SUFUSUFU negative regulator of hedgehog signaling | Sällan (1–4%) | I 1 tillstånd |
| TERTtelomerase reverse transcriptase | Sällan (1–4%) | I 1 tillstånd |
| TRAF7TNF receptor associated factor 7 | Sällan (1–4%) | I 1 tillstånd |
| ATL1atlastin GTPase 1 | Inte registrerat | I 1 tillstånd |
| ATXN10ataxin 10 | Inte registrerat | I 1 tillstånd |
| AUHAU RNA binding methylglutaconyl-CoA hydratase | Inte registrerat | I 1 tillstånd |
| CFAP43cilia and flagella associated protein 43 | Inte registrerat | I 1 tillstånd |
| CHMP2Bcharged multivesicular body protein 2B | Inte registrerat | I 1 tillstånd |
| COQ2coenzyme Q2, polyprenyltransferase | Inte registrerat | I 1 tillstånd |
| FLVCR1FLVCR choline and heme transporter 1 | Inte registrerat | I 1 tillstånd |
| FMR1fragile X messenger ribonucleoprotein 1 | Inte registrerat | I 1 tillstånd |
| FUZfuzzy planar cell polarity protein | Inte registrerat | I 1 tillstånd |
| GALNT2polypeptide N-acetylgalactosaminyltransferase 2 | Inte registrerat | I 1 tillstånd |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Inte registrerat | I 1 tillstånd |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Inte registrerat | I 1 tillstånd |
| IFT57intraflagellar transport 57 | Inte registrerat | I 1 tillstånd |
| IGHMBP2immunoglobulin mu DNA binding protein 2 | Inte registrerat | I 1 tillstånd |
| JAM2junctional adhesion molecule 2 | Inte registrerat | I 1 tillstånd |
| KIF5Akinesin family member 5A | Inte registrerat | I 1 tillstånd |
| MNX1motor neuron and pancreas homeobox 1 | Inte registrerat | I 1 tillstånd |
| MYORGmyogenesis regulating glycosidase | Inte registrerat | I 1 tillstånd |
| NAA60N-alpha-acetyltransferase 60, NatF catalytic subunit | Inte registrerat | I 1 tillstånd |
| PANK2pantothenate kinase 2 | Inte registrerat | I 1 tillstånd |
| PDGFRBplatelet derived growth factor receptor beta | Inte registrerat | I 1 tillstånd |
| PEX11Bperoxisomal biogenesis factor 11 beta | Inte registrerat | I 1 tillstånd |
| PRDM8PR/SET domain 8 | Inte registrerat | I 1 tillstånd |
| RETREG1reticulophagy regulator 1 | Inte registrerat | I 1 tillstånd |
| SCN9Asodium voltage-gated channel alpha subunit 9 | Inte registrerat | I 1 tillstånd |
| SLC20A2solute carrier family 20 member 2 | Inte registrerat | I 1 tillstånd |
| SLC9A6solute carrier family 9 member A6 | Inte registrerat | I 1 tillstånd |
| SPASTspastin | Inte registrerat | I 1 tillstånd |
| TBPTATA-box binding protein | Inte registrerat | I 1 tillstånd |
| TBXTT-box transcription factor T | Inte registrerat | I 1 tillstånd |
| TREM2triggering receptor expressed on myeloid cells 2 | Inte registrerat | I 1 tillstånd |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Inte registrerat | I 1 tillstånd |
| TTRtransthyretin | Inte registrerat | I 1 tillstånd |
| TYROBPtransmembrane immune signaling adaptor TYROBP | Inte registrerat | I 1 tillstånd |
| VANGL1VANGL planar cell polarity protein 1 | Inte registrerat | I 1 tillstånd |
| VANGL2VANGL planar cell polarity protein 2 | Inte registrerat | I 1 tillstånd |
| XPR1xenotropic and polytropic retrovirus receptor 1 | Inte registrerat | I 1 tillstånd |
| ZC4H2zinc finger C4H2-type containing | Inte registrerat | I 1 tillstånd |
| ZFYVE26zinc finger FYVE-type containing 26 | Inte registrerat | I 1 tillstånd |
Hur ofta det förekommer hos personer med ett av genens tillstånd, den vanligaste frekvensen bland dem, enligt Human Phenotype Ontology. Dessa sidor beskriver egenskaper och forskningen bakom dem. De är inte en diagnos, och det är läkare eller genetisk rådgivare du bör fråga om symtom.
Mer specifika egenskaper
Bredare egenskaper
Varifrån informationen kommer
- Human Phenotype Ontology, version 2026-09-01: egenskapen, dess namn, definition och de gener som är kopplade till den. Läs mer på hpo.jax.org.
- Dataversion 2026.10.19-9814e911.
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