VWA3B, von Willebrand factor A domain containing 3B

VWA3B, von Willebrand factor A domain containing 3B

• This gene encodes an intracellular protein that contains a von Willebrand factor type A domain. Intracellular proteins with VWA domains are thought to function in transcription, DNA repair, ribosomal and membrane transport and the proteasome. Mutations in this gene are associated with Spinocerebellar ataxia, autosomal recessive 22. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, May 2017]

• Gene Synonyms (von Willebrand factor A domain-containing protein 3B, VWA domain-containing protein 3B, SCAR22,)
• NCBI Gene ID: 200403
• Species: Homo sapiens (Human)
• UNIPROT ID#>>B7Z3D8
  UNIPROT ID#>>Q502W6
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

von Willebrand factor A domain containing 3B interacts with:

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.