calcium voltage-gated channel subunit alpha1 F

Preferred Label : calcium voltage-gated channel subunit alpha1 F;

Approved symbol HGNC : CACNA1F;

Alias symbols HGNC : OA2; JM8; CSNBX2; CSNB2A; JMC8; CORDX3; Cav1.4;

Chromosome HGNC : Xp11.23;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000102001;

Details

Origin ID

HGNC:1393;

UMLS CUI

C1413060;

Automatic exact mappings (from CISMeF team)
- Calcium channel, voltage-dependent, alpha-1f subunit [OMIM gene]
- Night blindness, congenital stationary, type 2a [OMIM Phenotype]
- calcium voltage-gated channel subunit alpha1 F [ORDO Gene]
OMIM gene
- Calcium channel, voltage-dependent, alpha-1f subunit [OMIM gene]
Orphanet gene
- calcium voltage-gated channel subunit alpha1 F [ORDO Gene]
See also inter- (CISMeF)
- Cone-rod dystrophy, X-linked, 3 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Calcium channel, voltage-dependent, alpha-1f subunit [OMIM gene]

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