Požymis
Gray matter heterotopia
Heterotopia or neuronal heterotopia are macroscopic clusters of misplaced neurons (gray matter), most often situated along the ventricular walls or within the subcortical white matter.
Santrauka
- Taip pat vadinama
- Gray matter heterotopias, Grey matter heterotopia, Grey matter heterotopias, Heterotopia, Heterotopias, Neuronal heterotopia
- Kūno sistema
- Abnormality of the nervous system
Atskaitos genomasGRCh38hg38
Pozicijos genų ir variantų puslapiuose rodomos pagal šį pasirinkimą šioje naršyklėje.
Read the genes linked to Gray matter heterotopia, and the rest of your genome, with one test.
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Įsigyti savo Genome Test97 genų susiję su Gray matter heterotopia
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Gray matter heterotopia. Dauguma žmonių, turinčių šį požymį, neturi nė vienos iš tų ligų, o šiame sąraše esantis genas nieko nesako apie kieno nors paties genomą.
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| ACTBactin beta | Visada | 1 ligoje |
| B4GAT1beta-1,4-glucuronyltransferase 1 | Visada | 1 ligoje |
| EML1EMAP like 1 | Visada | 1 ligoje |
| GPSM2G protein signaling modulator 2 | Visada | 2 ligose |
| MAP1Bmicrotubule associated protein 1B | Visada | 1 ligoje |
| NEDD4LNEDD4 like E3 ubiquitin protein ligase | Visada | 1 ligoje |
| PEX14peroxisomal biogenesis factor 14 | Visada | 1 ligoje |
| RAP1BRAP1B, member of RAS oncogene family | Visada | 1 ligoje |
| RNU4-2RNA, U4 small nuclear 2 | Visada | 1 ligoje |
| WSB2WD repeat and SOCS box containing 2 | Visada | 1 ligoje |
| ANKLE2ankyrin repeat and LEM domain containing 2 | Labai dažnai (80–99%) | 1 ligoje |
| ASPMassembly factor for spindle microtubules | Labai dažnai (80–99%) | 1 ligoje |
| CDK5RAP2CDK5 regulatory subunit associated protein 2 | Labai dažnai (80–99%) | 1 ligoje |
| CDK6cyclin dependent kinase 6 | Labai dažnai (80–99%) | 1 ligoje |
| CENPEcentromere protein E | Labai dažnai (80–99%) | 1 ligoje |
| CEP135centrosomal protein 135 | Labai dažnai (80–99%) | 1 ligoje |
| CEP152centrosomal protein 152 | Labai dažnai (80–99%) | 1 ligoje |
| CITcitron rho-interacting serine/threonine kinase | Labai dažnai (80–99%) | 1 ligoje |
| COPB2coat protein complex I subunit beta 2 | Labai dažnai (80–99%) | 1 ligoje |
| CPAPcentrosome assembly and centriole elongation protein | Labai dažnai (80–99%) | 1 ligoje |
| ERMARDER membrane associated RNA degradation | Labai dažnai (80–99%) | 1 ligoje |
| KIF14kinesin family member 14 | Labai dažnai (80–99%) | 1 ligoje |
| KNL1kinetochore scaffold 1 | Labai dažnai (80–99%) | 1 ligoje |
| MCM7minichromosome maintenance complex component 7 | Labai dažnai (80–99%) | 1 ligoje |
| MCPH1microcephalin 1 | Labai dažnai (80–99%) | 1 ligoje |
| METTL5methyltransferase 5, N6-adenosine | Labai dažnai (80–99%) | 1 ligoje |
| MFSD2AMFSD2 lysolipid transporter A, lysophospholipid | Labai dažnai (80–99%) | 1 ligoje |
| NCAPD3non-SMC condensin II complex subunit D3 | Labai dažnai (80–99%) | 1 ligoje |
| NUP37nucleoporin 37 | Labai dažnai (80–99%) | 1 ligoje |
| PDCD6IPprogrammed cell death 6 interacting protein | Labai dažnai (80–99%) | 1 ligoje |
| PHC1polyhomeotic homolog 1 | Labai dažnai (80–99%) | 1 ligoje |
| PYCR2pyrroline-5-carboxylate reductase 2 | Labai dažnai (80–99%) | 1 ligoje |
| SARS1seryl-tRNA synthetase 1 | Labai dažnai (80–99%) | 1 ligoje |
| SASS6SAS-6 centriolar assembly protein | Labai dažnai (80–99%) | 1 ligoje |
| STILSTIL centriolar assembly protein | Labai dažnai (80–99%) | 1 ligoje |
| TAF13TATA-box binding protein associated factor 13 | Labai dažnai (80–99%) | 1 ligoje |
| TRAPPC10trafficking protein particle complex subunit 10 | Labai dažnai (80–99%) | 1 ligoje |
| TRAPPC14trafficking protein particle complex subunit 14 | Labai dažnai (80–99%) | 1 ligoje |
| WARS1tryptophanyl-tRNA synthetase 1 | Labai dažnai (80–99%) | 1 ligoje |
| WDR62WD repeat domain 62 | Labai dažnai (80–99%) | 2 ligose |
Rodyti dar 57 genų
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| EPG5ectopic P-granules 5 autophagy tethering factor | Dažnai (30–79%) | 2 ligose |
| FKRPfukutin related protein | Dažnai (30–79%) | 2 ligose |
| GGT1gamma-glutamyltransferase 1 | Dažnai (30–79%) | 1 ligoje |
| GMPPBGDP-mannose pyrophosphorylase B | Dažnai (30–79%) | 1 ligoje |
| HNRNPKheterogeneous nuclear ribonucleoprotein K | Dažnai (30–79%) | 2 ligose |
| LAMB1laminin subunit beta 1 | Dažnai (30–79%) | 2 ligose |
| MAN2C1mannosidase alpha class 2C member 1 | Dažnai (30–79%) | 1 ligoje |
| MLH1mutL homolog 1 | Dažnai (30–79%) | 1 ligoje |
| PMS2PMS1 homolog 2, mismatch repair system component | Dažnai (30–79%) | 1 ligoje |
| POMGNT1protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | Dažnai (30–79%) | 1 ligoje |
| POMKprotein O-mannose kinase | Dažnai (30–79%) | 1 ligoje |
| POMT1protein O-mannosyltransferase 1 | Dažnai (30–79%) | 2 ligose |
| POMT2protein O-mannosyltransferase 2 | Dažnai (30–79%) | 1 ligoje |
| SLC4A10solute carrier family 4 member 10 | Dažnai (30–79%) | 1 ligoje |
| TCP1t-complex 1 | Dažnai (30–79%) | 1 ligoje |
| TMTC3transmembrane O-mannosyltransferase targeting cadherins 3 | Dažnai (30–79%) | 1 ligoje |
| UGGT1UDP-glucose glycoprotein glucosyltransferase 1 | Dažnai (30–79%) | 1 ligoje |
| ADD3adducin 3 | Kartais (5–29%) | 1 ligoje |
| AKT1AKT serine/threonine kinase 1 | Kartais (5–29%) | 1 ligoje |
| AKT3AKT serine/threonine kinase 3 | Kartais (5–29%) | 1 ligoje |
| ALG11ALG11 alpha-1,2-mannosyltransferase | Kartais (5–29%) | 1 ligoje |
| ARMC9armadillo repeat containing 9 | Kartais (5–29%) | 1 ligoje |
| CRB2crumbs cell polarity complex component 2 | Kartais (5–29%) | 1 ligoje |
| DCHS1dachsous cadherin-related 1 | Kartais (5–29%) | 2 ligose |
| FAT4FAT atypical cadherin 4 | Kartais (5–29%) | 2 ligose |
| FGFR3fibroblast growth factor receptor 3 | Kartais (5–29%) | 2 ligose |
| LMBRD2LMBR1 domain containing 2 | Kartais (5–29%) | 1 ligoje |
| MTORmechanistic target of rapamycin kinase | Kartais (5–29%) | 1 ligoje |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Kartais (5–29%) | 1 ligoje |
| PLCH1phospholipase C eta 1 | Kartais (5–29%) | 1 ligoje |
| PPFIBP1PPFIB scaffold protein 1 | Kartais (5–29%) | 1 ligoje |
| PPP1R12Aprotein phosphatase 1 regulatory subunit 12A | Kartais (5–29%) | 1 ligoje |
| RALGAPA1Ral GTPase activating protein catalytic subunit alpha 1 | Kartais (5–29%) | 1 ligoje |
| RNU2-2RNA, U2 small nuclear 2 | Kartais (5–29%) | 1 ligoje |
| RNU4ATACRNA, U4atac small nuclear | Kartais (5–29%) | 1 ligoje |
| SPENspen family transcriptional repressor | Kartais (5–29%) | 1 ligoje |
| TUBB2Btubulin beta 2B class IIb | Kartais (5–29%) | 1 ligoje |
| CRPPACDP-L-ribitol pyrophosphorylase A | Retai (1–4 %) | 2 ligose |
| FKTNfukutin | Retai (1–4 %) | 1 ligoje |
| ASXL1ASXL transcriptional regulator 1 | Neužfiksuota | 1 ligoje |
| BLTP1bridge-like lipid transfer protein family member 1 | Neužfiksuota | 1 ligoje |
| DCXdoublecortin | Neužfiksuota | 1 ligoje |
| FLNAfilamin A | Neužfiksuota | 1 ligoje |
| HYLS1HYLS1 centriolar and ciliogenesis associated | Neužfiksuota | 1 ligoje |
| KANSL1KAT8 regulatory NSL complex subunit 1 | Neužfiksuota | 1 ligoje |
| KIF2Akinesin family member 2A | Neužfiksuota | 1 ligoje |
| LAMA1laminin subunit alpha 1 | Neužfiksuota | 1 ligoje |
| MED12mediator complex subunit 12 | Neužfiksuota | 1 ligoje |
| MPDZmultiple PDZ domain crumbs cell polarity complex component | Neužfiksuota | 1 ligoje |
| OFD1OFD1 centriole and centriolar satellite protein | Neužfiksuota | 1 ligoje |
| PAFAH1B1platelet activating factor acetylhydrolase 1b regulatory subunit 1 | Neužfiksuota | 1 ligoje |
| PEX1peroxisomal biogenesis factor 1 | Neužfiksuota | 1 ligoje |
| SLC25A24solute carrier family 25 member 24 | Neužfiksuota | 1 ligoje |
| TMEM107transmembrane protein 107 | Neužfiksuota | 1 ligoje |
| TUBA1Atubulin alpha 1a | Neužfiksuota | 1 ligoje |
| USP18ubiquitin specific peptidase 18 | Neužfiksuota | 1 ligoje |
| ZSWIM6zinc finger SWIM-type containing 6 | Neužfiksuota | 1 ligoje |
Kaip dažnai šis požymis pasitaiko žmonėms, turintiems vieną iš geno sukeliamų ligų, ir kuris dažnis tarp jų didžiausias, pagal Žmogaus fenotipo ontologijos duomenis. Šiuose puslapiuose aprašomi požymiai ir juos grindžiantys tyrimai; tai nėra diagnozė, o su simptomais kreipkitės į gydytoją ar genetikos konsultantą.
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- Žmogaus fenotipo ontologija, 2026-09-01 leidimas: požymis, jo pavadinimai, apibrėžimas ir su juo susiję genai. Daugiau sužinokite svetainėje hpo.jax.org.
- Duomenų leidimas 2026.10.16-c6eea6bf.
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