XB-GENEPAGE-6041761
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vwa3b
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von Willebrand factor A domain containing 3B
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(
Nomenclature history )
AI Protein Function
:
Vwa3b encodes a secreted extracellular matrix protein that contains von Willebrand factor type A domains and is localized to the extracellular space.
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Diseases:
Disease Ontology:
autosomal recessive spinocerebellar ataxia 22
MIM:
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 22; SCAR22
External Links:
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