Known Diseases associated with this Protein: |  ALPORT SYNDROME, WITH MACROTHROMBOCYTOPENIA (APSM)
| DEAFNESS, AUTOSOMAL DOMINANT 17
| DEAFNESS, AUTOSOMAL DOMINANT, 17 (DFNA17)
| EPSTEIN SYNDROME
| EPSTEIN SYNDROME (EPS)
| EPSTEIN SYNDROME, INCLUDED
| EPSTEIN SYNDROME, INCLUDED;;
| FECHTNER SYNDROME
| FECHTNER SYNDROME (FTNS)
| FECHTNER SYNDROME, INCLUDED
| FECHTNER SYNDROME, INCLUDED;;
| MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS, INCLUD
| MAY-HEGGLIN ANOMALY
| MAY-HEGGLIN ANOMALY (MHA)
| MAY-HEGGLIN ANOMALY, INCLUDED
| SEBASTIAN SYNDROME
| SEBASTIAN SYNDROME (SBS)
| SEBASTIAN SYNDROME, INCLUDED
| SEBASTIAN SYNDROME, INCLUDED;;
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|  | Tips: The Domains on the Default View are decided by the Domain's E-Value. Clicking a check box will display or hide the correlated domain. To view the Gene page, either click on the link to the left or the blue bar above the Protein's graphic. |
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6166599
MYH9_HUMAN RecName: Full=Myosin-9; AltName: Full=Cellular myosin heavy chain, type A; AltName: Full=Myosin heavy chain 9; AltName: Full=Myosin heavy chain, non-muscle IIa; AltName: Full=Non-muscle myosin heavy chain A; Short=NMMHC-A; AltName: Full=Non-muscle myosin heavy chain IIa; Short=NMMHC II-a; Short=NMMHC-IIA
28
4
11
1
20