Heterogeneous nuclear ribonucleoprotein a2/b1

Preferred Label : Heterogeneous nuclear ribonucleoprotein a2/b1;

Symbol : HNRNPA2B1;

CISMeF acronym : HNRNPA2B1;

Type : Gene;

Alternative titles and symbols : HNRPA2B1;

Included titles and symbols : Heterogeneous nuclear ribonucleoprotein a2; Heterogeneous nuclear ribonucleoprotein b1; HNRPA2; HNRPB1;

Ensembl ID : ENSG00000122566;

Prefixed ID : *600124;

Details

Origin ID

600124;

UMLS CUI

C1415636;

Automatic exact mappings (from CISMeF team)
- HNRNPA2B1 Gene [NCIt concept]
- HNRNPA2B1 wt Allele [NCIt concept]
- Heterogeneous Nuclear Ribonucleoprotein A2/B1 [NCIt concept]
- Heterogeneous-Nuclear ribonucleoprotein group A-B [MeSH Descriptor]
- heterogeneous nuclear ribonucleoprotein A2/B1 [ORDO Gene]
- heterogeneous nuclear ribonucleoprotein A2/B1 [HGNC gene]
HGNC gene
- heterogeneous nuclear ribonucleoprotein A2/B1 [HGNC gene]
NCIt concept(s)
- HNRNPA2B1 Gene [NCIt concept]
- HNRNPA2B1 wt Allele [NCIt concept]
- Heterogeneous Nuclear Ribonucleoprotein A2/B1 [NCIt concept]
ORDO concept(s)
- heterogeneous nuclear ribonucleoprotein A2/B1 [ORDO Gene]
Phenotypes related
- Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 [OMIM Phenotype]
- Oculopharyngeal muscular dystrophy 2 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- HNRNPA2B1 Gene [NCIt concept]
- heterogeneous nuclear ribonucleoprotein A2/B1 [HGNC gene]

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