Solute carrier family 52 (riboflavin transporter), member 3

Preferred Label : Solute carrier family 52 (riboflavin transporter), member 3;

Symbol : SLC52A3;

CISMeF acronym : SLC52A3;

Type : Gene;

Alternative titles and symbols : Riboflavin transporter 2; Chromosome 20 open reading frame 54; RFT2; RFVT3; C20ORF54;

Ensembl ID : ENSG00000101276;

Prefixed ID : *613350;

Details

Origin ID

613350;

UMLS CUI

C1424064;

Automatic exact mappings (from CISMeF team)
- solute carrier family 52 member 3 [ORDO Gene]
- solute carrier family 52 member 3 [HGNC gene]
HGNC gene
- solute carrier family 52 member 3 [HGNC gene]
NCIt concept(s)
- SLC52A3 Gene [NCIt concept]
- SLC52A3 wt Allele [NCIt concept]
- Solute Carrier Family 52, Riboflavin Transporter, Member 3 [NCIt concept]
ORDO concept(s)
- solute carrier family 52 member 3 [ORDO Gene]
Phenotypes related
- Brown-vialetto-van laere syndrome 1 [OMIM Phenotype]
- Fazio-londe disease [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SLC52A3 Gene [NCIt concept]
- solute carrier family 52 member 3 [HGNC gene]

Keyword's position in hierarchy(ies) :

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