SLC22A3 wt Allele

Preferred Label : SLC22A3 wt Allele;

NCIt synonyms : EMT; OCT3; Solute Carrier Family 22 (Organic Cation Transporter), Member 3 wt Allele; EMTH;

NCIt definition : Human SLC22A3 wild-type allele is located in the vicinity of 6q25.3 and is approximately 107 kb in length. This allele, which encodes Solute carrier family 22 member 3 protein, plays a role in the disposition of cationic neurotoxins and neurotransmitters in the brain. Mutations in this gene are associated with extragonadal seminoma and placental choriocarcinoma.;

GenBank Accession Number : NM_021977;

Details

Origin ID

C113562;

UMLS CUI

C3812262;

Automatic exact mappings (from CISMeF team)
- Epithelial-to-mesenchymal transformation [FMA entity]
- IL2 inducible T cell kinase [ORDO Gene]
- Il2-inducible t-cell kinase [OMIM gene]
- Paramedic (occupation) [SNOMED CT concept]
- Pou domain, class 5, transcription factor 1 [OMIM gene]
- Solute carrier family 22 (extraneuronal monoamine transporter), member 3 [OMIM gene]
- epithelial to mesenchymal transition [GO term]
- thalamic eminence [UBERON concept]
OMIM relation
- Solute carrier family 22 (extraneuronal monoamine transporter), member 3 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_plays_role_in_process
- Ion Transport Process [NCIt concept]
- Ligand Binding [NCIt concept]
- Transmembrane Transport [NCIt concept]
- Transport Process [NCIt concept]
- Xenobiotic Metabolism [NCIt concept]

Keyword's position in hierarchy(ies) :

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