Solute carrier family 26 (sulfate transporter), member 2

Preferred Label : Solute carrier family 26 (sulfate transporter), member 2;

Symbol : SLC26A2;

CISMeF acronym : SLC26A2;

Type : Gene;

Alternative titles and symbols : Dtd sulfate transporter; DTDST;

Ensembl ID : ENSG00000155850;

Prefixed ID : *606718;

Détails

Origin ID

606718;

UMLS CUI

C1420162;

Automatic exact mappings (from CISMeF team)
- SLC26A2 gene [LOINC component]
- solute carrier family 26 member 2 [ORDO Gene]
- solute carrier family 26 member 2 [HGNC gene]
HGNC gene
- solute carrier family 26 member 2 [HGNC gene]
NCIt concept(s)
- SLC26A2 Gene [NCIt concept]
- SLC26A2 wt Allele [NCIt concept]
- Sulfate Transporter [NCIt concept]
ORDO concept(s)
- solute carrier family 26 member 2 [ORDO Gene]
Phenotypes related
- Achondrogenesis, type ib [OMIM Phenotype]
- Atelosteogenesis, type II [OMIM Phenotype]
- Diastrophic dysplasia [OMIM Phenotype]
- Epiphyseal dysplasia, multiple, 4 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SLC26A2 gene [LOINC component]
- solute carrier family 26 member 2 [HGNC gene]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients