Solute carrier family 31 (copper transporter), member 1

Preferred Label : Solute carrier family 31 (copper transporter), member 1;

Symbol : SLC31A1;

CISMeF acronym : SLC31A1;

Type : Gene;

Alternative titles and symbols : Copper transporter 1; COPT1; CTR1;

Ensembl ID : ENSG00000136868;

Prefixed ID : *603085;

Details

Origin ID

603085;

UMLS CUI

C1420182;

Automatic exact mappings (from CISMeF team)
- Copper Transporter 1 [MeSH Descriptor]
- High Affinity Copper Uptake Protein 1 [NCIt concept]
- SLC31A1 Gene [NCIt concept]
- SLC31A1 wt Allele [NCIt concept]
- copper transporter 1 [MeSH concept]
- solute carrier family 31 member 1 [HGNC gene]
HGNC gene
- solute carrier family 31 member 1 [HGNC gene]
NCIt concept(s)
- High Affinity Copper Uptake Protein 1 [NCIt concept]
- SLC31A1 Gene [NCIt concept]
- SLC31A1 wt Allele [NCIt concept]
Phenotypes related
- Neurodegeneration and seizures due to copper transport defect [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SLC31A1 Gene [NCIt concept]
- solute carrier family 31 member 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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