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Egenskap
Self-injurious behavior
Self-aggression.
Sammanfattning
- Även kallad
- Autoagression, Self injury, Self-harm, Self-injurious behaviors, Self-injurious behaviours
- Kroppssystem
- Abnormality of the nervous system
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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/self-injurious-behavior.json"
page <- fromJSON(url)
page$trait$nameSelf-injurious behaviorHP:0100716
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Läs generna kopplade till Self-injurious behavior, och resten av ditt genom, med ett enda test.
Från 449 $Fri frakt · Resultat inom 6–8 veckor
Beställ mitt Genome Test66 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Intellectual DisabilityReads 38 of these genesASXL3CRBNELP2FOXP1GRIA1GRIA3About this report →
- Epilepsy (Full Panel)Reads 28 of these genesGLSGRIA3GRIN1ATP6V0A1DNM1EEF1A2About this report →
- Tuberous SclerosisReads 2 of these genesTSC1TSC2About this report →
- Hereditary Episodic AtaxiasReads 2 of these genesKCNA1SCN2AAbout this report →
Show 62 more reports
- CDH2-Related ACOGSReads 1 of these genesCDH2About this report →
- CTNNB1 SyndromeReads 1 of these genesCTNNB1About this report →
- DeSanto-Shinawi SyndromeReads 1 of these genesWACAbout this report →
- Dias-Logan SyndromeReads 1 of these genesBCL11AAbout this report →
- Dyssegmental Dysplasia, Silverman-Handmaker TypeReads 1 of these genesHSPG2About this report →
- FAT4-Related Neurodevelopmental DisorderReads 1 of these genesFAT4About this report →
- Fragile X SyndromeReads 1 of these genesFMR1About this report →
- Glutaminase DeficiencyReads 1 of these genesGLSAbout this report →
- GRIA2-Related Neurodevelopmental DisorderReads 1 of these genesGRIA2About this report →
- Lamb-Shaffer SyndromeReads 1 of these genesSOX5About this report →
- Marshall-Smith SyndromeReads 1 of these genesNFIXAbout this report →
- Primrose SyndromeReads 1 of these genesZBTB20About this report →
- Radio-Tartaglia SyndromeReads 1 of these genesSPENAbout this report →
- RTTN-Related Microcephalic Primordial DwarfismReads 1 of these genesRTTNAbout this report →
- Schwartz-Jampel Syndrome Type 1Reads 1 of these genesHSPG2About this report →
- Smith-Lemli-Opitz SyndromeReads 1 of these genesDHCR7About this report →
- SPOP-Related Neurodevelopmental Disorder with MacrocephalyReads 1 of these genesSPOPAbout this report →
- Succinic Semialdehyde Dehydrogenase DeficiencyReads 1 of these genesALDH5A1About this report →
- TRIM8-Related Neurodevelopmental and Kidney DisorderReads 1 of these genesTRIM8About this report →
- Purine & Pyrimidine Metabolism DisordersReads 2 of these genesHPRT1DPYDAbout this report →
- Dent Disease and Lowe SyndromeReads 1 of these genesOCRLAbout this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 2 of these genesMAGEL2SNRPNAbout this report →
- Syndromic Complex Neurodevelopmental DisorderReads 3 of these genesRNU4-2AFG2AAP1S2About this report →
- Cerebral Creatine Deficiency SyndromesReads 1 of these genesGAMTAbout this report →
- Monogenic Precocious PubertyReads 1 of these genesMKRN3About this report →
- Neuroacanthocytosis and Huntington Disease PhenocopiesReads 1 of these genesVPS13AAbout this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 2 of these genesKIF5CTUBG1About this report →
- Complex Neurodevelopmental Disorder (TRRAP, MYH10, RERE, SOX11)Reads 1 of these genesREREAbout this report →
- Familial Atrial FibrillationReads 1 of these genesGJA5About this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesNFIXAbout this report →
- Autosomal Recessive Primary MicrocephalyReads 2 of these genesCEP152ASPMAbout this report →
- GPI Anchor Biosynthesis DefectsReads 2 of these genesPIGPPIGQAbout this report →
- Lissencephaly Spectrum DisordersReads 2 of these genesARXTUBG1About this report →
- Cornelia de Lange SyndromeReads 1 of these genesNIPBLAbout this report →
- VitreoretinopathyReads 2 of these genesCTNNB1NDPAbout this report →
- Oculocutaneous AlbinismReads 1 of these genesOCA2About this report →
- Autism Spectrum DisorderReads 1 of these genesCHD8About this report →
- Complex Neurodevelopmental Disorder With Motor FeaturesReads 1 of these genesELP2About this report →
- Marfan Like SyndromesReads 1 of these genesSKIAbout this report →
- Arrhythmogenic CardiomyopathyReads 1 of these genesCDH2About this report →
- BH4 Deficiency & Monoamine Neurotransmitter DisordersReads 1 of these genesMAOAAbout this report →
- Coffin-Siris SyndromeReads 1 of these genesSMARCC2About this report →
- Hypogonadotropic HypogonadismReads 2 of these genesMAGEL2SNRPNAbout this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 1 of these genesFAT4About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesATRXAbout this report →
- Hereditary Corneal DystrophiesReads 1 of these genesTCF4About this report →
- Pontocerebellar Hypoplasia (TSEN54 and MINPP1)Reads 1 of these genesTBC1D23About this report →
- Syndromic CraniosynostosisReads 1 of these genesSKIAbout this report →
- Inherited Neurodegenerative DisordersReads 4 of these genesFMR1NIPA1PNKPVPS13AAbout this report →
- Inherited IchthyosesReads 1 of these genesABCA12About this report →
- Hearing Loss and DeafnessReads 2 of these genesKARS1GJB2About this report →
- Congenital Myasthenic SyndromeReads 1 of these genesALG14About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesBCORAbout this report →
- Diabetes MellitusReads 1 of these genesZBTB20About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesGJB2About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesPNKPAbout this report →
- Dilated CardiomyopathyReads 1 of these genesPRDM16About this report →
- Female InfertilityReads 1 of these genesFMR1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesPNKPAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesPNKPVPS13AAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesNIPA1About this report →
- Congenital Disorders of GlycosylationReads 1 of these genesALG14About this report →
Läs generna kopplade till Self-injurious behavior, och resten av ditt genom, med ett enda test.
Från 449 $Fri frakt · Resultat inom 6–8 veckor
Beställ mitt Genome Test166 gener kopplade till Self-injurious behavior
Förändringar i dessa gener orsakar sällsynta tillstånd där Self-injurious behavior 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 |
|---|---|---|
| ALG14ALG14 UDP-N-acetylglucosaminyltransferase subunit | Alltid | I 1 tillstånd |
| ASXL3ASXL transcriptional regulator 3 | Alltid | I 1 tillstånd |
| CEP152centrosomal protein 152 | Alltid | I 1 tillstånd |
| CRBNcereblon | Alltid | I 1 tillstånd |
| ELP2elongator acetyltransferase complex subunit 2 | Alltid | I 1 tillstånd |
| FOXP1forkhead box P1 | Alltid | I 1 tillstånd |
| GLSglutaminase | Alltid | I 1 tillstånd |
| GRIA1glutamate ionotropic receptor AMPA type subunit 1 | Alltid | I 1 tillstånd |
| GRIA3glutamate ionotropic receptor AMPA type subunit 3 | Alltid | I 1 tillstånd |
| GRIN1glutamate ionotropic receptor NMDA type subunit 1 | Alltid | I 4 tillstånd |
| KARS1lysyl-tRNA synthetase 1 | Alltid | I 1 tillstånd |
| KDM6Blysine demethylase 6B | Alltid | I 1 tillstånd |
| KIF5Ckinesin family member 5C | Alltid | I 1 tillstånd |
| LRRC7leucine rich repeat containing 7 | Alltid | I 1 tillstånd |
| NEUROG1neurogenin 1 | Alltid | I 1 tillstånd |
| RNU4-2RNA, U4 small nuclear 2 | Alltid | I 1 tillstånd |
| SHQ1SHQ1, H/ACA ribonucleoprotein assembly factor | Alltid | I 1 tillstånd |
| SLC6A17solute carrier family 6 member 17 | Alltid | I 1 tillstånd |
| TM2D3TM2 domain containing 3 | Alltid | I 1 tillstånd |
| UGGT1UDP-glucose glycoprotein glucosyltransferase 1 | Alltid | I 1 tillstånd |
| YWHAZtyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta | Alltid | I 1 tillstånd |
| HERC2HECT and RLD domain containing E3 ubiquitin protein ligase 2 | Mycket ofta (80–99 %) | I 1 tillstånd |
| HPRT1hypoxanthine phosphoribosyltransferase 1 | Mycket ofta (80–99 %) | I 1 tillstånd |
| MAGEL2MAGE family member L2 | Mycket ofta (80–99 %) | I 4 tillstånd |
| MKRN3makorin ring finger protein 3 | Mycket ofta (80–99 %) | I 1 tillstånd |
| NPAP1nuclear pore associated protein 1 | Mycket ofta (80–99 %) | I 1 tillstånd |
| PWAR1Prader Willi/Angelman region RNA 1 | Mycket ofta (80–99 %) | I 1 tillstånd |
| PWRN1Prader-Willi region non-protein coding RNA 1 | Mycket ofta (80–99 %) | I 1 tillstånd |
| RAI1retinoic acid induced 1 | Mycket ofta (80–99 %) | I 1 tillstånd |
| SNORD115-1small nucleolar RNA, C/D box 115-1 | Mycket ofta (80–99 %) | I 1 tillstånd |
| SNORD116-1small nucleolar RNA, C/D box 116-1 | Mycket ofta (80–99 %) | I 1 tillstånd |
| SYT1synaptotagmin 1 | Mycket ofta (80–99 %) | I 1 tillstånd |
| AHDC1AT-hook DNA binding motif containing 1 | Ofta (30–79 %) | I 1 tillstånd |
| ATP6V0A1ATPase H+ transporting V0 subunit a1 | Ofta (30–79 %) | I 1 tillstånd |
| CASZ1castor zinc finger 1 | Ofta (30–79 %) | I 1 tillstånd |
| CHD8chromodomain helicase DNA binding protein 8 | Ofta (30–79 %) | I 1 tillstånd |
| CLCN3Cl-/H+ antiporter 3 | Ofta (30–79 %) | I 1 tillstånd |
| DHCR77-dehydrocholesterol reductase | Ofta (30–79 %) | I 1 tillstånd |
| DNM1dynamin 1 | Ofta (30–79 %) | I 1 tillstånd |
| EEF1A2eukaryotic translation elongation factor 1 alpha 2 | Ofta (30–79 %) | I 1 tillstånd |
Visa 126 gener till
| Gen | Hur ofta den förekommer | Tillstånd |
|---|---|---|
| FBXW11F-box and WD repeat domain containing 11 | Ofta (30–79 %) | I 1 tillstånd |
| FEM1Bfem-1 homolog B | Ofta (30–79 %) | I 1 tillstånd |
| GABBR2gamma-aminobutyric acid type B receptor subunit 2 | Ofta (30–79 %) | I 1 tillstånd |
| GABRDgamma-aminobutyric acid type A receptor subunit delta | Ofta (30–79 %) | I 1 tillstånd |
| HDAC4histone deacetylase 4 | Ofta (30–79 %) | I 1 tillstånd |
| HSPG2heparan sulfate proteoglycan 2 | Ofta (30–79 %) | I 1 tillstånd |
| IFNGinterferon gamma | Ofta (30–79 %) | I 1 tillstånd |
| KCNAB2potassium voltage-gated channel subfamily A regulatory beta subunit 2 | Ofta (30–79 %) | I 1 tillstånd |
| KPTNkaptin, actin binding protein | Ofta (30–79 %) | I 2 tillstånd |
| LUZP1leucine zipper protein 1 | Ofta (30–79 %) | I 1 tillstånd |
| MBD5methyl-CpG binding domain protein 5 | Ofta (30–79 %) | I 2 tillstånd |
| MMP23Bmatrix metallopeptidase 23B | Ofta (30–79 %) | I 1 tillstånd |
| MSL2MSL complex subunit 2 | Ofta (30–79 %) | I 1 tillstånd |
| NAA80N-alpha-acetyltransferase 80, NatH catalytic subunit | Ofta (30–79 %) | I 1 tillstånd |
| NDNnecdin, MAGE family member | Ofta (30–79 %) | I 3 tillstånd |
| NDST1N-deacetylase and N-sulfotransferase 1 | Ofta (30–79 %) | I 1 tillstånd |
| NIPBLNIPBL cohesin loading factor | Ofta (30–79 %) | I 1 tillstånd |
| NRCAMneuronal cell adhesion molecule | Ofta (30–79 %) | I 1 tillstånd |
| NTNG2netrin G2 | Ofta (30–79 %) | I 1 tillstånd |
| OCA2OCA2 melanosomal transmembrane protein | Ofta (30–79 %) | I 3 tillstånd |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Ofta (30–79 %) | I 1 tillstånd |
| PDPNpodoplanin | Ofta (30–79 %) | I 1 tillstånd |
| POGZpogo transposable element derived with ZNF domain | Ofta (30–79 %) | I 2 tillstånd |
| PRDM16PR/SET domain 16 | Ofta (30–79 %) | I 1 tillstånd |
| PRKCZprotein kinase C zeta | Ofta (30–79 %) | I 1 tillstånd |
| RBL2RB transcriptional corepressor like 2 | Ofta (30–79 %) | I 1 tillstånd |
| REREarginine-glutamic acid dipeptide repeats | Ofta (30–79 %) | I 2 tillstånd |
| RNU2-2RNA, U2 small nuclear 2 | Ofta (30–79 %) | I 1 tillstånd |
| RPL10ribosomal protein L10 | Ofta (30–79 %) | I 1 tillstånd |
| SKISKI proto-oncogene | Ofta (30–79 %) | I 1 tillstånd |
| SLC32A1solute carrier family 32 member 1 | Ofta (30–79 %) | I 2 tillstånd |
| SMARCC2SWI/SNF related BAF chromatin remodeling complex subunit C2 | Ofta (30–79 %) | I 1 tillstånd |
| SNRPNsmall nuclear ribonucleoprotein polypeptide N | Ofta (30–79 %) | I 3 tillstånd |
| SPENspen family transcriptional repressor | Ofta (30–79 %) | I 1 tillstånd |
| SPOPspeckle type BTB/POZ protein | Ofta (30–79 %) | I 1 tillstånd |
| TSC1TSC complex subunit 1 | Ofta (30–79 %) | I 1 tillstånd |
| TSC2TSC complex subunit 2 | Ofta (30–79 %) | I 1 tillstånd |
| UBAP2Lubiquitin associated protein 2 like | Ofta (30–79 %) | I 1 tillstånd |
| UBE2Aubiquitin conjugating enzyme E2 A | Ofta (30–79 %) | I 1 tillstånd |
| UBE4Bubiquitination factor E4B | Ofta (30–79 %) | I 1 tillstånd |
| WASF1WASP family member 1 | Ofta (30–79 %) | I 1 tillstånd |
| WASHC4WASH complex subunit 4 | Ofta (30–79 %) | I 1 tillstånd |
| ZBTB20zinc finger and BTB domain containing 20 | Ofta (30–79 %) | I 1 tillstånd |
| ABCA12ATP binding cassette subfamily A member 12 | Ibland (5–29 %) | I 1 tillstånd |
| ACBD6acyl-CoA binding domain containing 6 | Ibland (5–29 %) | I 1 tillstånd |
| AP1G1adaptor related protein complex 1 subunit gamma 1 | Ibland (5–29 %) | I 1 tillstånd |
| ARXaristaless related homeobox | Ibland (5–29 %) | I 1 tillstånd |
| ASPMassembly factor for spindle microtubules | Ibland (5–29 %) | I 1 tillstånd |
| ATRXATRX chromatin remodeler | Ibland (5–29 %) | I 1 tillstånd |
| BCL11ABCL11 transcription factor A | Ibland (5–29 %) | I 1 tillstånd |
| BCORBCL6 corepressor | Ibland (5–29 %) | I 1 tillstånd |
| CACNA1Ecalcium voltage-gated channel subunit alpha1 E | Ibland (5–29 %) | I 1 tillstånd |
| CASKcalcium/calmodulin dependent serine protein kinase | Ibland (5–29 %) | I 1 tillstånd |
| CDC42BPBCDC42 binding protein kinase beta | Ibland (5–29 %) | I 1 tillstånd |
| CDH2cadherin 2 | Ibland (5–29 %) | I 1 tillstånd |
| CDKL5cyclin dependent kinase like 5 | Ibland (5–29 %) | I 1 tillstånd |
| CHD5chromodomain helicase DNA binding protein 5 | Ibland (5–29 %) | I 1 tillstånd |
| CHKAcholine kinase alpha | Ibland (5–29 %) | I 1 tillstånd |
| CLCN4Cl-/H+ antiporter 4 | Ibland (5–29 %) | I 1 tillstånd |
| CREBBPCREB binding lysine acetyltransferase | Ibland (5–29 %) | I 2 tillstånd |
| CTNNB1catenin beta 1 | Ibland (5–29 %) | I 1 tillstånd |
| DCHS1dachsous cadherin-related 1 | Ibland (5–29 %) | I 1 tillstånd |
| DMXL2Dmx like 2 | Ibland (5–29 %) | I 1 tillstånd |
| DPYDdihydropyrimidine dehydrogenase | Ibland (5–29 %) | I 1 tillstånd |
| EHMT1euchromatic histone lysine methyltransferase 1 | Ibland (5–29 %) | I 1 tillstånd |
| EP300EP300 lysine acetyltransferase | Ibland (5–29 %) | I 1 tillstånd |
| FAT4FAT atypical cadherin 4 | Ibland (5–29 %) | I 1 tillstånd |
| FMR1fragile X messenger ribonucleoprotein 1 | Ibland (5–29 %) | I 1 tillstånd |
| GAMTguanidinoacetate N-methyltransferase | Ibland (5–29 %) | I 1 tillstånd |
| GJB2gap junction protein beta 2 | Ibland (5–29 %) | I 1 tillstånd |
| GNAO1G protein subunit alpha o1 | Ibland (5–29 %) | I 2 tillstånd |
| GRM7glutamate metabotropic receptor 7 | Ibland (5–29 %) | I 1 tillstånd |
| HECW2HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2 | Ibland (5–29 %) | I 1 tillstånd |
| HNRNPH2heterogeneous nuclear ribonucleoprotein H2 | Ibland (5–29 %) | I 1 tillstånd |
| IQSEC2IQ motif and Sec7 domain ArfGEF 2 | Ibland (5–29 %) | I 1 tillstånd |
| KCNA1potassium voltage-gated channel subfamily A member 1 | Ibland (5–29 %) | I 1 tillstånd |
| KICS2KICSTOR subunit 2 | Ibland (5–29 %) | I 1 tillstånd |
| KIF15kinesin family member 15 | Ibland (5–29 %) | I 1 tillstånd |
| KMT2Clysine methyltransferase 2C | Ibland (5–29 %) | I 2 tillstånd |
| LGI1leucine rich glioma inactivated 1 | Ibland (5–29 %) | I 1 tillstånd |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Ibland (5–29 %) | I 1 tillstånd |
| NDPnorrin cystine knot growth factor NDP | Ibland (5–29 %) | I 1 tillstånd |
| NEUROD2neuronal differentiation 2 | Ibland (5–29 %) | I 1 tillstånd |
| NFIXnuclear factor I X | Ibland (5–29 %) | I 1 tillstånd |
| NIPA1NIPA magnesium transporter 1 | Ibland (5–29 %) | I 1 tillstånd |
| NIPA2NIPA magnesium transporter 2 | Ibland (5–29 %) | I 1 tillstånd |
| ODC1ornithine decarboxylase 1 | Ibland (5–29 %) | I 1 tillstånd |
| PIDD1p53-induced death domain protein 1 | Ibland (5–29 %) | I 1 tillstånd |
| PIGPphosphatidylinositol glycan anchor biosynthesis class P | Ibland (5–29 %) | I 1 tillstånd |
| PIGQphosphatidylinositol glycan anchor biosynthesis class Q | Ibland (5–29 %) | I 1 tillstånd |
| PNKPpolynucleotide kinase 3'-phosphatase | Ibland (5–29 %) | I 1 tillstånd |
| PPFIA3PPFI scaffold protein A3 | Ibland (5–29 %) | I 1 tillstånd |
| PPP2CAprotein phosphatase 2 catalytic subunit alpha | Ibland (5–29 %) | I 1 tillstånd |
| RFX7regulatory factor X7 | Ibland (5–29 %) | I 1 tillstånd |
| RHOBTB2Rho related BTB domain containing 2 | Ibland (5–29 %) | I 2 tillstånd |
| RNU5B-1RNA, U5B small nuclear 1 | Ibland (5–29 %) | I 1 tillstånd |
| RPS6KA3ribosomal protein S6 kinase A3 | Ibland (5–29 %) | I 1 tillstånd |
| RTTNrotatin | Ibland (5–29 %) | I 1 tillstånd |
| SCAF4SR-related CTD associated factor 4 | Ibland (5–29 %) | I 1 tillstånd |
| SCN1Bsodium voltage-gated channel beta subunit 1 | Ibland (5–29 %) | I 1 tillstånd |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Ibland (5–29 %) | I 1 tillstånd |
| SETBP1SET binding protein 1 | Ibland (5–29 %) | I 1 tillstånd |
| SIK1salt inducible kinase 1 | Ibland (5–29 %) | I 1 tillstånd |
| SLC25A22solute carrier family 25 member 22 | Ibland (5–29 %) | I 1 tillstånd |
| SOX5SRY-box transcription factor 5 | Ibland (5–29 %) | I 1 tillstånd |
| TAOK1TAO kinase 1 | Ibland (5–29 %) | I 1 tillstånd |
| TBC1D23TBC1 domain family member 23 | Ibland (5–29 %) | I 1 tillstånd |
| TCF4transcription factor 4 | Ibland (5–29 %) | I 2 tillstånd |
| TKTtransketolase | Ibland (5–29 %) | I 2 tillstånd |
| TMEM147transmembrane protein 147 | Ibland (5–29 %) | I 1 tillstånd |
| TRIM8tripartite motif containing 8 | Ibland (5–29 %) | I 1 tillstånd |
| TRIOtrio Rho guanine nucleotide exchange factor | Ibland (5–29 %) | I 1 tillstånd |
| TUBG1tubulin gamma 1 | Ibland (5–29 %) | I 1 tillstånd |
| VAMP2vesicle associated membrane protein 2 | Ibland (5–29 %) | I 1 tillstånd |
| VPS13Avacuolar protein sorting 13 homolog A | Ibland (5–29 %) | I 1 tillstånd |
| WACWW domain containing adaptor with coiled-coil | Ibland (5–29 %) | I 1 tillstånd |
| WDR83OSWD repeat domain 83 opposite strand | Ibland (5–29 %) | I 1 tillstånd |
| AFG2AAAA ATPase AFG2A | Sällan (1–4%) | I 1 tillstånd |
| GJA5gap junction protein alpha 5 | Sällan (1–4%) | I 1 tillstånd |
| GJA8gap junction protein alpha 8 | Sällan (1–4%) | I 1 tillstånd |
| GRIA2glutamate ionotropic receptor AMPA type subunit 2 | Sällan (1–4%) | I 1 tillstånd |
| ALDH5A1aldehyde dehydrogenase 5 family member A1 | Inte registrerat | I 1 tillstånd |
| AP1S2adaptor related protein complex 1 subunit sigma 2 | Inte registrerat | I 1 tillstånd |
| KMT2Elysine methyltransferase 2E (inactive) | Inte registrerat | I 1 tillstånd |
| MAOAmonoamine oxidase A | Inte registrerat | I 1 tillstånd |
| RLIMring finger protein, LIM domain interacting | 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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