DDX11 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human DDX11 wild-type allele is located in the vicinity of 12p11.21 and is approximately 31 kb in length. This allele, which encodes ATP-dependent DNA helicase DDX11 protein, is involved in DNA replication, DNA repair, heterochromatin organization and ribosomal RNA synthesis. Mutation of the gene is associated with Warsaw breakage syndrome.

**Synonyms:** - CHL1 - CHL1-Like Helicase Homolog (S. cerevisiae) Gene - CHL1-Like Helicase Homolog Gene - CHL1-Related Helicase Gene 1 - CHLR1 - ChlR1 - DEAD/H (Asp-Glu-Ala-Asp/His) Box Helicase 11 Gene - DEAD/H (Asp-Glu-Ala-Asp/His) Box Polypeptide 11 (CHL1-Like Helicase Homolog, S. cerevisiae) Gene - DEAD/H (Asp-Glu-Ala-Asp/His) Box Polypeptide 11 (S.cerevisiae CHL1-Like Helicase) Gene - DEAD/H (Asp-Glu-Ala-Asp/His) Box Polypeptide 11 Gene - DEAD/H-Box 11 Gene - DEAD/H-Box Helicase 11 wt Allele - KRG-2 - KRG2 - Keratinocyte Growth Factor Regulated Gene 2 - Keratinocyte Growth Factor-Regulated Gene 2 - Probable ATP-Dependent DNA Helicase DDX11 Gene - Probable ATP-Dependent RNA Helicase DDX11 Gene - WABS - Warsaw Breakage Syndrome Gene