Atrx chromatin remodeler

Preferred Label : Atrx chromatin remodeler;

Symbol : ATRX;

CISMeF acronym : ATRX;

Type : Gene;

Alternative titles and symbols : Helicase 2, X-linked; X-linked nuclear protein gene; XH2; XNP; Atr-X gene;

Ensembl ID : ENSG00000085224;

Prefixed ID : *300032;

Details

Origin ID

300032;

UMLS CUI

C1412697;

Automatic exact mappings (from CISMeF team)
- ATRX Gene [NCIt concept]
- ATRX chromatin remodeler [ORDO Gene]
- ATRX chromatin remodeler [HGNC gene]
- ATRX gene [LOINC component]
- ATRX wt Allele [NCIt concept]
- Alpha Thalassemia X-Linked Mental Retardation Syndrome [NCIt concept]
- Transcriptional Regulator ATRX [NCIt concept]
HGNC gene
- ATRX chromatin remodeler [HGNC gene]
NCIt concept(s)
- ATRX Gene [NCIt concept]
- ATRX wt Allele [NCIt concept]
- Transcriptional Regulator ATRX [NCIt concept]
ORDO concept(s)
- ATRX chromatin remodeler [ORDO Gene]
Phenotypes related
- Alpha-thalassemia myelodysplasia syndrome [OMIM Phenotype]
- Alpha-thalassemia/impaired intellectual development syndrome, X-linked [OMIM Phenotype]
- Intellectual disability-hypotonic facies syndrome, X-linked, 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- ATRX Gene [NCIt concept]
- ATRX chromatin remodeler [HGNC gene]
- ATRX gene [LOINC component]

Keyword's position in hierarchy(ies) :

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