Presku: | AAP48072 |
Size: | 100 ug |
Weight: | 226kDa |
Gene: | 4627 |
Format: | Lyophilized powder |
Target: | MYH9 is 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. |
Alternative names: | DFNA17; EPSTS; FTNS; MGC104539; MHA; NMHC-II-A; NMMHCA |