Search
Search
Proteintech
{{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.promotions']}}
{{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.viewpromo']}}
{{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.promocode']}}: {{promo.promoCode}} {{promo.promoTitle}} {{promo.promoDescription}}. {{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.learnmore']}}
Immunogen sequence: NINALPDVS VDDVRSTSQG LSSFKPLPRP PPLAQGNDLP LGQPRKLGRE DLQPPSSTPS CSGTVFSAPQ NRSPPAGTAP TPGTSSAQDL PSSPIYASVS PANPSSKRPL DAHLALVNQH PIGPFPRVQS PPHLKSPSAE ATVAGGCLLP PSPSGHPDQT GTNQHFVMVE VHRPDSEPDV NEVRALPQTR TSTLSQLSDS GQTLSEDSGV DAGEAEASAP GRGRQSASTK SRSSKELPRN ERPTDGANKP PGLLEPTSTL VRVKKSAATL GIAIEGGANT RQPLPRIVTI QRGGSAHNCG QLKVGHVILE VNGLTLRGKE HREAARIIAE AFKTKDRDYI DFLVTEFNVM L (558-907 aa encoded by BC014524)
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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: Autosomal recessive deafness type 31 protein; CASK-interacting protein CIP98; deafness, autosomal recessive 31; Whirlin
基因别名: CIP98; DFNB31; KIAA1526; PDZD7B; USH2D; WHRN; WI
UniProt ID: (Human) Q9P202
Entrez Gene ID: (Human) 25861