Tunnus
Self-injurious behavior
Self-aggression.
Kokkuvõte
- Teised nimetused
- Autoagression, Self injury, Self-harm, Self-injurious behaviors, Self-injurious behaviours
- Kehasüsteem
- Abnormality of the nervous system
Selle lehe andmed
Lehe aadressile saab lisada .json või päringusse application/json, et lugeda seda JSON-vormingus.
library(jsonlite)
url <- "https://dantelabs.com/traits/self-injurious-behavior.json"
page <- fromJSON(url)
page$trait$nameLugege välja geenid, mis on seotud Self-injurious behavior-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test166 geeni on seotud tunnusega Self-injurious behavior
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Self-injurious behavior. 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 |
|---|---|---|
| ALG14ALG14 UDP-N-acetylglucosaminyltransferase subunit | Alati | Esineb 1 haiguses |
| ASXL3ASXL transcriptional regulator 3 | Alati | Esineb 1 haiguses |
| CEP152centrosomal protein 152 | Alati | Esineb 1 haiguses |
| CRBNcereblon | Alati | Esineb 1 haiguses |
| ELP2elongator acetyltransferase complex subunit 2 | Alati | Esineb 1 haiguses |
| FOXP1forkhead box P1 | Alati | Esineb 1 haiguses |
| GLSglutaminase | Alati | Esineb 1 haiguses |
| GRIA1glutamate ionotropic receptor AMPA type subunit 1 | Alati | Esineb 1 haiguses |
| GRIA3glutamate ionotropic receptor AMPA type subunit 3 | Alati | Esineb 1 haiguses |
| GRIN1glutamate ionotropic receptor NMDA type subunit 1 | Alati | Esineb 4 haiguses |
| KARS1lysyl-tRNA synthetase 1 | Alati | Esineb 1 haiguses |
| KDM6Blysine demethylase 6B | Alati | Esineb 1 haiguses |
| KIF5Ckinesin family member 5C | Alati | Esineb 1 haiguses |
| LRRC7leucine rich repeat containing 7 | Alati | Esineb 1 haiguses |
| NEUROG1neurogenin 1 | Alati | Esineb 1 haiguses |
| RNU4-2RNA, U4 small nuclear 2 | Alati | Esineb 1 haiguses |
| SHQ1SHQ1, H/ACA ribonucleoprotein assembly factor | Alati | Esineb 1 haiguses |
| SLC6A17solute carrier family 6 member 17 | Alati | Esineb 1 haiguses |
| TM2D3TM2 domain containing 3 | Alati | Esineb 1 haiguses |
| UGGT1UDP-glucose glycoprotein glucosyltransferase 1 | Alati | Esineb 1 haiguses |
| YWHAZtyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta | Alati | Esineb 1 haiguses |
| HERC2HECT and RLD domain containing E3 ubiquitin protein ligase 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| HPRT1hypoxanthine phosphoribosyltransferase 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| MAGEL2MAGE family member L2 | Väga sageli (80–99%) | Esineb 4 haiguses |
| MKRN3makorin ring finger protein 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| NPAP1nuclear pore associated protein 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PWAR1Prader Willi/Angelman region RNA 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PWRN1Prader-Willi region non-protein coding RNA 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| RAI1retinoic acid induced 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SNORD115-1small nucleolar RNA, C/D box 115-1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SNORD116-1small nucleolar RNA, C/D box 116-1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SYT1synaptotagmin 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| AHDC1AT-hook DNA binding motif containing 1 | Sageli (30–79%) | Esineb 1 haiguses |
| ATP6V0A1ATPase H+ transporting V0 subunit a1 | Sageli (30–79%) | Esineb 1 haiguses |
| CASZ1castor zinc finger 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CHD8chromodomain helicase DNA binding protein 8 | Sageli (30–79%) | Esineb 1 haiguses |
| CLCN3Cl-/H+ antiporter 3 | Sageli (30–79%) | Esineb 1 haiguses |
| DHCR77-dehydrocholesterol reductase | Sageli (30–79%) | Esineb 1 haiguses |
| DNM1dynamin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| EEF1A2eukaryotic translation elongation factor 1 alpha 2 | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 126 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| FBXW11F-box and WD repeat domain containing 11 | Sageli (30–79%) | Esineb 1 haiguses |
| FEM1Bfem-1 homolog B | Sageli (30–79%) | Esineb 1 haiguses |
| GABBR2gamma-aminobutyric acid type B receptor subunit 2 | Sageli (30–79%) | Esineb 1 haiguses |
| GABRDgamma-aminobutyric acid type A receptor subunit delta | Sageli (30–79%) | Esineb 1 haiguses |
| HDAC4histone deacetylase 4 | Sageli (30–79%) | Esineb 1 haiguses |
| HSPG2heparan sulfate proteoglycan 2 | Sageli (30–79%) | Esineb 1 haiguses |
| IFNGinterferon gamma | Sageli (30–79%) | Esineb 1 haiguses |
| KCNAB2potassium voltage-gated channel subfamily A regulatory beta subunit 2 | Sageli (30–79%) | Esineb 1 haiguses |
| KPTNkaptin, actin binding protein | Sageli (30–79%) | Esineb 2 haiguses |
| LUZP1leucine zipper protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| MBD5methyl-CpG binding domain protein 5 | Sageli (30–79%) | Esineb 2 haiguses |
| MMP23Bmatrix metallopeptidase 23B | Sageli (30–79%) | Esineb 1 haiguses |
| MSL2MSL complex subunit 2 | Sageli (30–79%) | Esineb 1 haiguses |
| NAA80N-alpha-acetyltransferase 80, NatH catalytic subunit | Sageli (30–79%) | Esineb 1 haiguses |
| NDNnecdin, MAGE family member | Sageli (30–79%) | Esineb 3 haiguses |
| NDST1N-deacetylase and N-sulfotransferase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NIPBLNIPBL cohesin loading factor | Sageli (30–79%) | Esineb 1 haiguses |
| NRCAMneuronal cell adhesion molecule | Sageli (30–79%) | Esineb 1 haiguses |
| NTNG2netrin G2 | Sageli (30–79%) | Esineb 1 haiguses |
| OCA2OCA2 melanosomal transmembrane protein | Sageli (30–79%) | Esineb 3 haiguses |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Sageli (30–79%) | Esineb 1 haiguses |
| PDPNpodoplanin | Sageli (30–79%) | Esineb 1 haiguses |
| POGZpogo transposable element derived with ZNF domain | Sageli (30–79%) | Esineb 2 haiguses |
| PRDM16PR/SET domain 16 | Sageli (30–79%) | Esineb 1 haiguses |
| PRKCZprotein kinase C zeta | Sageli (30–79%) | Esineb 1 haiguses |
| RBL2RB transcriptional corepressor like 2 | Sageli (30–79%) | Esineb 1 haiguses |
| REREarginine-glutamic acid dipeptide repeats | Sageli (30–79%) | Esineb 2 haiguses |
| RNU2-2RNA, U2 small nuclear 2 | Sageli (30–79%) | Esineb 1 haiguses |
| RPL10ribosomal protein L10 | Sageli (30–79%) | Esineb 1 haiguses |
| SKISKI proto-oncogene | Sageli (30–79%) | Esineb 1 haiguses |
| SLC32A1solute carrier family 32 member 1 | Sageli (30–79%) | Esineb 2 haiguses |
| SMARCC2SWI/SNF related BAF chromatin remodeling complex subunit C2 | Sageli (30–79%) | Esineb 1 haiguses |
| SNRPNsmall nuclear ribonucleoprotein polypeptide N | Sageli (30–79%) | Esineb 3 haiguses |
| SPENspen family transcriptional repressor | Sageli (30–79%) | Esineb 1 haiguses |
| SPOPspeckle type BTB/POZ protein | Sageli (30–79%) | Esineb 1 haiguses |
| TSC1TSC complex subunit 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TSC2TSC complex subunit 2 | Sageli (30–79%) | Esineb 1 haiguses |
| UBAP2Lubiquitin associated protein 2 like | Sageli (30–79%) | Esineb 1 haiguses |
| UBE2Aubiquitin conjugating enzyme E2 A | Sageli (30–79%) | Esineb 1 haiguses |
| UBE4Bubiquitination factor E4B | Sageli (30–79%) | Esineb 1 haiguses |
| WASF1WASP family member 1 | Sageli (30–79%) | Esineb 1 haiguses |
| WASHC4WASH complex subunit 4 | Sageli (30–79%) | Esineb 1 haiguses |
| ZBTB20zinc finger and BTB domain containing 20 | Sageli (30–79%) | Esineb 1 haiguses |
| ABCA12ATP binding cassette subfamily A member 12 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ACBD6acyl-CoA binding domain containing 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| AP1G1adaptor related protein complex 1 subunit gamma 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ARXaristaless related homeobox | Mõnikord (5–29%) | Esineb 1 haiguses |
| ASPMassembly factor for spindle microtubules | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATRXATRX chromatin remodeler | Mõnikord (5–29%) | Esineb 1 haiguses |
| BCL11ABCL11 transcription factor A | Mõnikord (5–29%) | Esineb 1 haiguses |
| BCORBCL6 corepressor | Mõnikord (5–29%) | Esineb 1 haiguses |
| CACNA1Ecalcium voltage-gated channel subunit alpha1 E | Mõnikord (5–29%) | Esineb 1 haiguses |
| CASKcalcium/calmodulin dependent serine protein kinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| CDC42BPBCDC42 binding protein kinase beta | Mõnikord (5–29%) | Esineb 1 haiguses |
| CDH2cadherin 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CDKL5cyclin dependent kinase like 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CHD5chromodomain helicase DNA binding protein 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CHKAcholine kinase alpha | Mõnikord (5–29%) | Esineb 1 haiguses |
| CLCN4Cl-/H+ antiporter 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CREBBPCREB binding lysine acetyltransferase | Mõnikord (5–29%) | Esineb 2 haiguses |
| CTNNB1catenin beta 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DCHS1dachsous cadherin-related 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DMXL2Dmx like 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DPYDdihydropyrimidine dehydrogenase | Mõnikord (5–29%) | Esineb 1 haiguses |
| EHMT1euchromatic histone lysine methyltransferase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| EP300EP300 lysine acetyltransferase | Mõnikord (5–29%) | Esineb 1 haiguses |
| FAT4FAT atypical cadherin 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FMR1fragile X messenger ribonucleoprotein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GAMTguanidinoacetate N-methyltransferase | Mõnikord (5–29%) | Esineb 1 haiguses |
| GJB2gap junction protein beta 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GNAO1G protein subunit alpha o1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| GRM7glutamate metabotropic receptor 7 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HECW2HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HNRNPH2heterogeneous nuclear ribonucleoprotein H2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IQSEC2IQ motif and Sec7 domain ArfGEF 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KCNA1potassium voltage-gated channel subfamily A member 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KICS2KICSTOR subunit 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KIF15kinesin family member 15 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KMT2Clysine methyltransferase 2C | Mõnikord (5–29%) | Esineb 2 haiguses |
| LGI1leucine rich glioma inactivated 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| NDPnorrin cystine knot growth factor NDP | Mõnikord (5–29%) | Esineb 1 haiguses |
| NEUROD2neuronal differentiation 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NFIXnuclear factor I X | Mõnikord (5–29%) | Esineb 1 haiguses |
| NIPA1NIPA magnesium transporter 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NIPA2NIPA magnesium transporter 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ODC1ornithine decarboxylase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PIDD1p53-induced death domain protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PIGPphosphatidylinositol glycan anchor biosynthesis class P | Mõnikord (5–29%) | Esineb 1 haiguses |
| PIGQphosphatidylinositol glycan anchor biosynthesis class Q | Mõnikord (5–29%) | Esineb 1 haiguses |
| PNKPpolynucleotide kinase 3'-phosphatase | Mõnikord (5–29%) | Esineb 1 haiguses |
| PPFIA3PPFI scaffold protein A3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PPP2CAprotein phosphatase 2 catalytic subunit alpha | Mõnikord (5–29%) | Esineb 1 haiguses |
| RFX7regulatory factor X7 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RHOBTB2Rho related BTB domain containing 2 | Mõnikord (5–29%) | Esineb 2 haiguses |
| RNU5B-1RNA, U5B small nuclear 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RPS6KA3ribosomal protein S6 kinase A3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RTTNrotatin | Mõnikord (5–29%) | Esineb 1 haiguses |
| SCAF4SR-related CTD associated factor 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SCN1Bsodium voltage-gated channel beta subunit 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SETBP1SET binding protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SIK1salt inducible kinase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC25A22solute carrier family 25 member 22 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SOX5SRY-box transcription factor 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TAOK1TAO kinase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TBC1D23TBC1 domain family member 23 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TCF4transcription factor 4 | Mõnikord (5–29%) | Esineb 2 haiguses |
| TKTtransketolase | Mõnikord (5–29%) | Esineb 2 haiguses |
| TMEM147transmembrane protein 147 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TRIM8tripartite motif containing 8 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TRIOtrio Rho guanine nucleotide exchange factor | Mõnikord (5–29%) | Esineb 1 haiguses |
| TUBG1tubulin gamma 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| VAMP2vesicle associated membrane protein 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| VPS13Avacuolar protein sorting 13 homolog A | Mõnikord (5–29%) | Esineb 1 haiguses |
| WACWW domain containing adaptor with coiled-coil | Mõnikord (5–29%) | Esineb 1 haiguses |
| WDR83OSWD repeat domain 83 opposite strand | Mõnikord (5–29%) | Esineb 1 haiguses |
| AFG2AAAA ATPase AFG2A | Harva (1–4%) | Esineb 1 haiguses |
| GJA5gap junction protein alpha 5 | Harva (1–4%) | Esineb 1 haiguses |
| GJA8gap junction protein alpha 8 | Harva (1–4%) | Esineb 1 haiguses |
| GRIA2glutamate ionotropic receptor AMPA type subunit 2 | Harva (1–4%) | Esineb 1 haiguses |
| ALDH5A1aldehyde dehydrogenase 5 family member A1 | Pole registreeritud | Esineb 1 haiguses |
| AP1S2adaptor related protein complex 1 subunit sigma 2 | Pole registreeritud | Esineb 1 haiguses |
| KMT2Elysine methyltransferase 2E (inactive) | Pole registreeritud | Esineb 1 haiguses |
| MAOAmonoamine oxidase A | Pole registreeritud | Esineb 1 haiguses |
| RLIMring finger protein, LIM domain interacting | Pole registreeritud | Esineb 1 haiguses |
Kui sageli see esineb geenist tulenevate seisunditega inimeste seas, kõige sagedamini nende kõigi seas, nagu on märgitud Inimese fenotüübi ontoloogias. Need lehed kirjeldavad tunnuseid ja nende taga olevaid uuringuid; need ei ole diagnoos ning sümptomite kohta tuleks küsida arstilt või geneetilt nõustajalt.
Kitsamad tunnused
Laiemad tunnused
Allikas
- Inimese fenotüübi ontoloogia, versioon 2026-09-01: tunnus, selle nimetused, määratlus ja sellega seotud geenid. Lisateave leiab aadressilt hpo.jax.org.
- Andmeversioon 2026.10.17-8666dff2.
Üks test. Vastused kogu eluks.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast