heterogeneous nuclear ribonucleoprotein A1

Preferred Label : heterogeneous nuclear ribonucleoprotein A1;

Approved symbol HGNC : HNRNPA1;

Alias symbols HGNC : ALS20; hnRNP-A1;

Chromosome HGNC : 12q13.13;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000135486;

Details

Origin ID

HGNC:5031;

UMLS CUI

C1415634;

Automatic exact mappings (from CISMeF team)
- Amyotrophic lateral sclerosis 20 [OMIM Phenotype]
- 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 [OMIM gene]
NCIt concept
- HNRNPA1 Gene [NCIt concept]
OMIM gene
- Heterogeneous nuclear ribonucleoprotein a1 [OMIM gene]
Orphanet gene
- heterogeneous nuclear ribonucleoprotein A1 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- HNRNPA1 Gene [NCIt concept]
- Heterogeneous nuclear ribonucleoprotein a1 [OMIM gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients