Heterogeneous nuclear ribonucleoprotein h2

Preferred Label : Heterogeneous nuclear ribonucleoprotein h2;

Symbol : HNRNPH2;

CISMeF acronym : HNRNPH2;

Type : Gene;

Alternative titles and symbols : Heterogeneous nuclear ribonucleoprotein h-prime; HNRPH2;

Ensembl ID : ENSG00000126945;

Prefixed ID : *300610;

Details

Origin ID

300610;

UMLS CUI

C1845100;

Automatic exact mappings (from CISMeF team)
- HNRNPH2 wt Allele [NCIt concept]
- Heterogeneous Nuclear Ribonucleoprotein H2 [NCIt concept]
- heterogeneous nuclear ribonucleoprotein H2 [HGNC gene]
HGNC gene
- heterogeneous nuclear ribonucleoprotein H2 [HGNC gene]
NCIt concept(s)
- HNRNPH2 Gene [NCIt concept]
- HNRNPH2 wt Allele [NCIt concept]
- Heterogeneous Nuclear Ribonucleoprotein H2 [NCIt concept]
Phenotypes related
- Intellectual developmental disorder, X-linked, syndromic, bain type [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- HNRNPH2 Gene [NCIt concept]
- heterogeneous nuclear ribonucleoprotein H2 [HGNC gene]

Keyword's position in hierarchy(ies) :

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