SLC52A2 wt Allele

Preferred Label : SLC52A2 wt Allele;

NCIt synonyms : FLJ11856; Solute Carrier Family 52 (Riboflavin Transporter), Member 2 Gene; G Protein-Coupled Receptor 172A Gene; hRFT3; GPR172A; RFVT2; Porcine Endogenous Retrovirus, Subgroup A, Receptor 1 Gene; Putative G-Protein Coupled Receptor GPCR41 Gene; Solute Carrier Family 52 Member 2 wt Allele; BVVLS2; D15Ertd747e; PAR1; RFT3; GPCR41; HuPAR-1; Solute Carrier Family 52, Riboflavin Transporter, Member 2 Gene;

NCIt definition : Human SLC52A2 wild-type allele is located in the vicinity of 8q24.3 and is approximately 27 kb in length. This allele, which encodes solute carrier family 52, riboflavin transporter, member 2 protein, is involved in cellular uptake of riboflavin in the brain and may play a role in retroviral receptor activity. Mutation of the gene is associated with Brown-Vialetto-Van Laere syndrome 2.;

NCI Metathesaurus CUI : CL1905154;

GenBank Accession Number : AY070774;

Details

Origin ID

C191792;

UMLS CUI

C5780793;

OMIM relation
- Solute carrier family 52 (riboflavin transporter), member 2 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 8q24.3 [NCIt concept]
gene_plays_role_in_process
- Ligand Binding [NCIt concept]
- Transmembrane Transport [NCIt concept]
- Transport Process [NCIt concept]
- Virus-Cell Membrane Interaction [NCIt concept]

Keyword's position in hierarchy(ies) :

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