Solute carrier family 46 (folate transporter), member 1

Preferred Label : Solute carrier family 46 (folate transporter), member 1;

Symbol : SLC46A1;

CISMeF acronym : SLC46A1;

Type : Gene;

Alternative titles and symbols : Heme carrier protein 1; Proton-coupled folate transporter; HCP1; PCFT;

Ensembl ID : ENSG00000076351;

Prefixed ID : *611672;

Details

Origin ID

611672;

UMLS CUI

C1968832;

Automatic exact mappings (from CISMeF team)
- PRMT1 wt Allele [NCIt concept]
- Proton-Coupled Folate Transporter [NCIt concept]
- Proton-Coupled folate transporter [MeSH concept]
- Proton-Coupled folate transporter [MeSH Descriptor]
- SLC46A1 Gene [NCIt concept]
- SLC46A1 wt Allele [NCIt concept]
- centromere protein F [ORDO Gene]
- solute carrier family 46 member 1 [ORDO Gene]
- solute carrier family 46 member 1 [HGNC gene]
HGNC gene
- solute carrier family 46 member 1 [HGNC gene]
NCIt concept(s)
- Proton-Coupled Folate Transporter [NCIt concept]
- SLC46A1 Gene [NCIt concept]
- SLC46A1 wt Allele [NCIt concept]
ORDO concept(s)
- solute carrier family 46 member 1 [ORDO Gene]
Phenotypes related
- Folate malabsorption, hereditary [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SLC46A1 Gene [NCIt concept]
- solute carrier family 46 member 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients