Heterogeneous nuclear ribonucleoprotein a1

Preferred Label : Heterogeneous nuclear ribonucleoprotein a1;

Symbol : HNRNPA1;

CISMeF acronym : HNRNPA1;

Type : Gene;

Alternative titles and symbols : Nuclear ribonucleoprotein particle a1 protein; HNRPA1;

Ensembl ID : ENSG00000135486;

Prefixed ID : *164017;

Détails

Origin ID

164017;

UMLS CUI

C1415634;

Automatic exact mappings (from CISMeF team)
- Heterogeneous Nuclear Ribonucleoprotein A1 [MeSH Descriptor]
- Heterogeneous Nuclear Ribonucleoprotein A1 [NCIt concept]
- heterogeneous nuclear ribonucleoprotein A1 [ORDO Gene]
Currated CISMeF NLP mapping
- HNRNPA1 Gene [NCIt concept]
- heterogeneous nuclear ribonucleoprotein A1 [HGNC gene]
HGNC gene
- heterogeneous nuclear ribonucleoprotein A1 [HGNC gene]
NCIt concept(s)
- HNRNPA1 Gene [NCIt concept]
- HNRNPA1 wt Allele [NCIt concept]
- Heterogeneous Nuclear Ribonucleoprotein A1 [NCIt concept]
ORDO concept(s)
- heterogeneous nuclear ribonucleoprotein A1 [ORDO Gene]
Phenotypes related
- Amyotrophic lateral sclerosis 20 [OMIM Phenotype]
- Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 [OMIM Phenotype]
- Myopathy, distal, 3 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- HNRNPA1 Gene [NCIt concept]
- heterogeneous nuclear ribonucleoprotein A1 [HGNC gene]
Validated automatic mappings to BTNT
- HNRNPA1 wt Allele [NCIt concept]

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