USH1G_MOUSE Q80T11
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UniProt:Q80T11
Recommended name：Usher syndrome type-1G protein homolog
EC number：
Alternative names：(Jackson shaker protein) (Scaffold protein containing ankyrin repeats and SAM domain)
Cleaved into：
GeneID：16470
Gene names (primary )：Ush1g
Gene names (synonym )：Sans
Gene names (ORF )：
Length：461
Mass：51490
Sequence：MNDQYHRAARDGYLELLKEATRKELNAPDEDGMTPTLWAAYHGNLESLRLIVSRGGDPDKCDIWGNTPLHLAASNGHLHCLSFLVSFGANIWCLDNDYHTPLDMAAMKGHMECVRYLDSIAAKQSSLNPKLVGKLKDKAFREAERRIRECAKMQRKHHERMERRYRRELAERSDTLSFSSLTSSTLSRRLQHMTLGSQLPYSQATLHGTAKGKAKIQKKLERRKQGGEGTFKVSEDGRKSVRSLSGLQLGSDVMFVRQGTYANPKEWGRAPLRDMFLSDEDSVSRATLAAEPAHSEVSTDSGHDSLFTRPGLGTMVFRRNYVSSGLHGLGREDGGLDGAGTPRGRLHSSPSLDDDSLGSANSLQDRSCGEELPWDELDLGLDEDLEPETSPLETFLASLHMEDFASLLRHEKIDLEALMLCSDLDLRSISVPLGPRKKILGAVRRRRQALERPLALEDTEL
Tissue specificity：Detected in stereocilia from cochlear hair cells (at protein level). Highly expressed in the cochlea, testis, cerebellum and eye, and low levels in brain, thymus and spleen. Significant signals detected in the neurosensory epithelium of inner ear cochlea and saccule, especially in inner and outer hair cells. {ECO:0000269|PubMed:12588793, ECO:0000269|PubMed:21436032, ECO:0000269|PubMed:21709241}.
Induction：
Developmental stage：Low-level expression detected in 17.5 dpc embryos but not in embryos earlier than 15.5 dpc.
Protein families：