NBS1 wt Allele

Cancer Terms -> Gene -> DNA Repair Gene -> NBS1 Gene -> NBS1 wt Allele

NBS1 wt Allele Definition

Human NBN wild-type allele is located within 8q21 and is approximately 51 kb in length. This allele, which encodes nibrin protein, is involved in DNA double-strand break repair and DNA damage-induced checkpoint activation. Functional mutations in the NBN gene produce allelic variants that are involved in Nijmegen breakage syndrome.

NBS1 wt Allele Synonyms

NBN wt Allele, AT-V1 Gene, AT-V2 Gene, ATV Gene, NALP2, NBS, NBS1, Nibrin wt Allele, Nijmegen Breakage Syndrome 1 (Nibrin) Gene, Nijmegen Breakage Syndrome 1 Gene, PYPAF2

Terms in NBS1 wt Allele category

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