Aliases for MYL7 Gene
External Ids for MYL7 Gene
Previous GeneCards Identifiers for MYL7 Gene
GeneCards Summary for MYL7 Gene
MYL7 (Myosin, Light Chain 7, Regulatory) is a Protein Coding gene. Diseases associated with MYL7 include fechtner syndrome and familial atrial fibrillation. Among its related pathways are Regulation of actin cytoskeleton and RhoGDI Pathway. GO annotations related to this gene include calcium ion binding. An important paralog of this gene is MYL12A.
Myosins are a large family of motor proteins that share the common features of ATP hydrolysis (ATPase enzyme activity), actin binding and potential for kinetic energy transduction. Originally isolated from muscle cells, almost all eukaryotic cells are known to contain myosins.