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Factor·arcadia

VWA8 protein

Von Willebrand factor A domain-containing protein 8; a mitochondrial matrix ATPase. Human mutations are associated with a subtype of retinitis pigmentosa; knockdown in zebrafish leads to retinal cell defects.

Confidence
70%
active

Source

Ciona model selection and gene prioritization

Connections (2)

VWA8 mutations cause retinitis pigmentosa via mitophagyAssociation
Mutated VWA8 causes developmental delay and skeletal defectsAssociation