transient receptor potential cation channel subfamily M member 1

Preferred Label : transient receptor potential cation channel subfamily M member 1;

Approved symbol HGNC : TRPM1;

Alias symbols HGNC : LTRPC1; CSNB1C;

Chromosome HGNC : 15q13.3;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000134160;

Details

Origin ID

HGNC:7146;

UMLS CUI

C1417194;

Automatic exact mappings (from CISMeF team)
- Night blindness, congenital stationary, type 1c [OMIM Phenotype]
- Transient receptor potential cation channel, subfamily M, member 1 [OMIM gene]
- transient receptor potential cation channel subfamily M member 1 [ORDO Gene]
OMIM gene
- Transient receptor potential cation channel, subfamily M, member 1 [OMIM gene]
Orphanet gene
- transient receptor potential cation channel subfamily M member 1 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Transient receptor potential cation channel, subfamily M, member 1 [OMIM gene]

Keyword's position in hierarchy(ies) :

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