| Health / Medical Topics |
WT2 wt Allele
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. (NCI Thesaurus)
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This gene may play a role in the regulation of gene expression.
