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XB-GENEPAGE-6041761
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vwa3b
???displayGene.name???:
von Willebrand factor A domain containing 3B
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(
Nomenclature history )
AI Protein Function
:
The gene vwa3b encodes a protein with von Willebrand factor A domains, involved in cell adhesion and may play a role in embryonic development. It is expressed in the notochord and somites. The protein ...[+]
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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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Symbol legend:
