C101341Level 5
ARVCF wt Allele
**Semantic type:** Gene or Genome
**Definition:** Human ARVCF wild-type allele is located in the vicinity of 22q11.21 and is approximately 47 kb in length. This allele, which encodes splicing regulator ARVCF protein, plays a role in mRNA splicing and cell-cell adhesion. Mutation of the gene is associated with velo-cardio-facial syndrome.
**Synonyms:** - ARVCF Delta Catenin Family Member wt Allele - Armadillo Repeat Gene Deleted in VCFS - Armadillo Repeat Gene Deleted in Velocardiofacial Syndrome Gene - FLJ35345
GET
/api/v1/systems/nci_thesaurus/nodes/C101341Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.