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VWA3B

Official Full Name
von Willebrand factor A domain containing 3B
Organism
Homo sapiens
GeneID
200403
Background
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]
Synonyms
SCAR22;

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