蛋白质/抗原/多肽 >> 重组蛋白
重组常染色体隐性遗传性耳聋型31蛋白
半岛bd体育手机客户端 介绍
基因名：
WHRN 半岛bd体育手机客户端 别名： CIP98； DFNB31； PDZD7B； USH2D； WI； WHRN； whirlin； whirlin； whirlin； CASK-interacting protein CIP98； autosomal recessive deafness type 31 protein； 常染色体隐性遗传性耳聋型31蛋白； 背景信息：
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.[provided by RefSeq, Mar 2010]
标签：His-tag |
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