World Of Taxonomy
C213722Level 6

DHX9 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human DHX9 wild-type allele is located in the vicinity of 1q25.3 and is approximately 49 kb in length. This allele, which encodes ATP-dependent RNA helicase A protein, plays a role in DNA and RNA helicase activity, transcriptional coactivation, DNA replication, alternative splicing of select genes, mRNA translation and responses to viral double-stranded RNA. Mutations in the gene are associated with autosomal dominant intellectual developmental disorder 75.

**Synonyms:** - DDX9 - DEAD/H (Asp-Glu-Ala-Asp/His) Box Polypeptide 9 Gene - DEAD/H-Box 9 Gene - DEAH (Asp-Glu-Ala-His) Box Helicase 9 Gene - DEAH (Asp-Glu-Ala-His) Box Polypeptide 9 Gene - DEAH-Box Helicase 9 Gene - DExH-Box Helicase 9 wt Allele - LKP - MRD75 - NDH II - NDH2 - NDHII - RHA

GET/api/v1/systems/nci_thesaurus/nodes/C213722
Official DownloadCC BY 4.0Source

Hierarchy Explorer

Loading...

Cross-system equivalences0

No cross-system equivalences mapped for this node.