WT2 wt Allele - CISMeF

Preferred Label : WT2 wt Allele;

Obsolete resource : true;

NCIt synonyms : WIT-2; MTACR1; WIT2; Wilms Tumor 2 wt Allele; ADCR;

NCIt definition : Human WT2 wild-type allele is located in the vicinity of 11p15.5 and its length has not been determined. This allele, which encodes an unknown protein, is putatively involved in the inhibition of cell growth. WT2 gene dysfunction is associated with nephroblastoma and Wiedemann-Beckwith syndrome.;

NCIt note : Fri Jul 07 13:42:12 EDT 2017 - HGNC reports Locus Type phenotype only and EntrezGene reports Gene type unknown.See 'WT2 Gene(C18263)';

Concept status : Retired_Concept;

Détails

Origin ID

C49436;

UMLS CUI

C1704668;

Automatic exact mappings (from CISMeF team)
- WT1 transcription factor [ORDO Gene]
OMIM relation
- Wilms tumor 2 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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

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