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myh9

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Official Full Name
myosin, heavy chain 9, non-muscle
Background
This gene encodes a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain. The protein is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in MYH9 are the cause of non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness.
Synonyms
MYH9; myosin, heavy chain 9, non-muscle; DFNA17, myosin, heavy polypeptide 9, non muscle; myosin-9; EPSTS; FTNS; MHA; NMHC II A; NMMHCA; nonmuscle myosin heavy chain II A; myosin heavy chain 9; non-muscle myosin heavy chain A; non-muscle myosin heavy cha; non-muscle myosin heavy chain IIa; nonmuscle myosin heavy chain II-A; myosin heavy chain, non-muscle IIa; cellular myosin heavy chain, type A; non-muscle myosin heavy polypeptide 9; BDPLT6; DFNA17; NMHC-II-A; NMMHC-IIA; MGC104539; NMMHC; myosin; nonmuscle; non-muscle; type A; NMMHC-A; NMMHC II-a; non-muscle IIa; heavy polypeptide 9; myosin heavy chain, nonmuscle; non