KEGG   VARIANT: 4635v1
Entry
4635v1                      Variant                                
Name
MYL4 mutation
Type
Loss of function
Gene
MYL4  myosin light chain 4 [KO:K12750]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 160770
Network
nt06539  Cytoskeleton in muscle cells
Disease
H00731  Atrial fibrillation
Reference
  Authors
Orr N, Arnaout R, Gula LJ, Spears DA, Leong-Sit P, Li Q, Tarhuni W, Reischauer S, Chauhan VS, Borkovich M, Uppal S, Adler A, Coughlin SR, Stainier DY, Gollob MH
  Title
A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation.
  Journal
Nat Commun 7:11303 (2016)
DOI:10.1038/ncomms11303
LinkDB

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