SLC52A1 wt Allele

Preferred Label : SLC52A1 wt Allele;

NCIt synonyms : RFT1; PAR2; G-Protein Coupled Receptor 42 Gene; FLJ10060; Solute Carrier Family 52 (Riboflavin Transporter), Member 1 Gene; GPCR42; huPAR-2; hRFT1; G Protein-Coupled Receptor 172B Gene; GPR172B; RFVT1; Solute Carrier Family 52, Riboflavin Transporter, Member 1 Gene; Porcine Endogenous Retrovirus, Subgroup A, Receptor 2 Gene; RBFVD; Solute Carrier Family 52 Member 1 wt Allele;

NCIt definition : Human SLC52A1 wild-type allele is located in the vicinity of 17p13.2 and is approximately 19 kb in length. This allele, which encodes solute carrier family 52, riboflavin transporter, member 1 protein, plays a role in the uptake of vitamin B2. Maternal haploinsufficiency of this gene is associated with transient neonatal riboflavin deficiency.;

NCI Metathesaurus CUI : CL1905152;

GenBank Accession Number : AY070775;

Details

Origin ID

C191798;

UMLS CUI

C5780794;

OMIM relation
- Solute carrier family 52 (riboflavin transporter), member 1 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 17p13.2 [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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