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簡(jiǎn)要描述：The protein encoded by this gene localizes to the primary cilium and to the plasma membrane. The gene functions in centriole migration to the apical membrane and formation of the primary cilium. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6). [provided by RefSeq, Nov 2008]
產(chǎn)品型號(hào)：bsm-62769R廠商性質(zhì)：生產(chǎn)廠家更新時(shí)間：2025-03-04訪 問(wèn) 量： 156產(chǎn)品分類(lèi)
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