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The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms.
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Protein Aliases: Autosomal recessive deafness type 31 protein; CASK-interacting protein CIP98; deafness, autosomal recessive 31; whirler; Whirlin
Gene Aliases: 1110035G07Rik; AW122018; AW742671; C430046P22Rik; CIP98; DFNB31; KIAA1526; PDZD7B; USH2D; WHRN; WI
UniProt ID: (Human) Q9P202, (Mouse) Q80VW4
Entrez Gene ID: (Human) 25861, (Mouse) 73750
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