CUL4B wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human CUL4B wild-type allele is located in the vicinity of Xq23 and is approximately 51 kb in length. This allele, which encodes cullin-4B protein, is involved in the mediation of protein ubiquitination. Mutation of the gene is associated with both mental retardation, X-linked, syndromic type 15 and Cabezas syndrome.

**Synonyms:** - Cullin 4B wt Allele - DKFZp686F1470 - KIAA0695 - MRXHF2 - MRXSC - SFM2