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FIGURE: 1 / 1
Positive Samples: U-87MG, HeLa, K-562, Mouse liver
Immunogen sequence: PSGHPDQTGT NQHFVMVEVH RPDSEPDVNE VRALPQTRTA STLSQLSDSG QTLSEDSGVD AGEAEASAPG RGRQSVSTKS RSSKELPRNE RPTDGANKPP GLLEPTSTLV RVKKSAATLG IAIEGGANTR QPLPRIVTIQ RGGSAHNCGQ LKVGHVILEV NGLTLRGKEH REAARIIAEA FKTKDRDYID FLVTEFNVML
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.
⚠WARNING: This product can expose you to chemicals including mercury, which is known to the State of California to cause birth defects or other reproductive harm. For more information go to www.P65Warnings.ca.gov.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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) Q80VW5
Entrez Gene ID: (Human) 25861, (Mouse) 73750
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