Disease-gene associations mined from literature

MYH9 disease associations

MYH9 [ENSP00000216181]

Cellular myosin heavy chain, type A; Cellular myosin that appears to play a role in cytokinesis, cell shape, and specialized functions such as secretion and capping. During cell spreading, plays an important role in cytoskeleton reorganization, focal contacts formation (in the margins but not the central part of spreading cells), and lamellipodial retraction; this function is mechanically antagonized by MYH10; Deafness associated genes

Synonyms:  MYH9,  MYH9p,  hMYH9,  A0A024R1N1,  B1AH99 ...

Linkouts:  STRING  Pharos  UniProt  OMIM