Solute carrier family 35 (udp-n-acetylglucosamine transporter), member 3

Preferred Label : Solute carrier family 35 (udp-n-acetylglucosamine transporter), member 3;

Symbol : SLC35A3;

CISMeF acronym : SLC35A3;

Type : Gene;

Alternative titles and symbols : Udp-n-acetylglucosamine transporter; Udp-glcnac transporter;

Ensembl ID : ENSG00000117620;

Prefixed ID : *605632;

Details

Origin ID

605632;

UMLS CUI

C1420189;

Automatic exact mappings (from CISMeF team)
- UDP-N-acetylglucosamine transport [GO term]
- UDP-N-acetylglucosamine transporter [MeSH concept]
- UDP-N-acetylglucosamine transporter [MeSH Supplementary Concept]
- solute carrier family 35 member A3 [HGNC gene]
- solute carrier family 35 member A3 [ORDO Gene]
HGNC gene
- solute carrier family 35 member A3 [HGNC gene]
ORDO concept(s)
- solute carrier family 35 member A3 [ORDO Gene]
Phenotypes related
- Arthrogryposis, impaired intellectual development, and seizures [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SLC35A3 gene [LOINC component]
- solute carrier family 35 member A3 [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients