Full name: von Willebrand factor A domain containing 3B

Gene type: protein coding

RefSeq status: REVIEWED

Also known as: SCAR22

Summary: 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]

Expression: Restricted expression toward testis (RPKM 15.5)

Gene size: 243450bp

Exon count: 37