Solute carrier family 22 (organic cation transporter), member 18

Preferred Label : Solute carrier family 22 (organic cation transporter), member 18;

Symbol : SLC22A18;

CISMeF acronym : SLC22A18;

Type : Gene;

Alternative titles and symbols : Solute carrier family 22 (organic cation transporter), member 1-like; Beckwith-wiedemann syndrome chromosome region 1, candidate a; Beckwith-wiedemann region 1a; Imprinted polyspecific membrane transporter 1; Organic-cation transporter-like 2; Tumor-suppressing subchromosomal transferable fragment candidate gene 5; SLC22A1L; BWSCR1A; BWR1A; IMPT1; ORCTL2; TSSC5;

Included titles and symbols : Beckwith-wiedemann syndrome critical region;

Ensembl ID : ENSG00000110628;

Prefixed ID : *602631;

Details

Origin ID

602631;

UMLS CUI

C1420135;

Automatic exact mappings (from CISMeF team)
- SLC22A18 Gene [NCIt concept]
- SLC22A18 gene [LOINC component]
- SLC22A18 wt Allele [NCIt concept]
- Solute Carrier Family 22 Member 18 [NCIt concept]
- solute carrier family 22 member 18 [ORDO Gene]
- solute carrier family 22 member 18 [HGNC gene]
HGNC gene
- solute carrier family 22 member 18 [HGNC gene]
NCIt concept(s)
- Organic Cation Transporter-Like 2 Protein [NCIt concept]
- SLC22A18 Gene [NCIt concept]
- SLC22A18 wt Allele [NCIt concept]
- Solute Carrier Family 22 Member 18 [NCIt concept]
ORDO concept(s)
- solute carrier family 22 member 18 [ORDO Gene]
Phenotypes related
- Breast cancer [OMIM Phenotype]
- Lung cancer [OMIM Phenotype]
- Rhabdomyosarcoma, embryonal, 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SLC22A18 Gene [NCIt concept]
- SLC22A18 gene [LOINC component]
- solute carrier family 22 member 18 [HGNC gene]

Keyword's position in hierarchy(ies) :

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