KEGG   VARIANT: 71v1
Entry
71v1                      Variant                                  
Name
ACTG1mutation
Gene
ACTG1  actin gamma 1 [KO:K05692]
Organism
hsa_var Human gene variants (Homo sapiens)
Network
nt06539  Cytoskeleton in muscle cells
Disease
H00604  Deafness, autosomal dominant
H02023  Baraitser-Winter syndrome
Reference
  Authors
Riviere JB, van Bon BW, Hoischen A, Kholmanskikh SS, O'Roak BJ, Gilissen C, Gijsen S, Sullivan CT, Christian SL, Abdul-Rahman OA, Atkin JF, Chassaing N, Drouin-Garraud V, Fry AE, Fryns JP, Gripp KW, Kempers M, Kleefstra T, Mancini GM, Nowaczyk MJ, van Ravenswaaij-Arts CM, Roscioli T, Marble M, Rosenfeld JA, Siu VM, de Vries BB, Shendure J, Verloes A, Veltman JA, Brunner HG, Ross ME, Pilz DT, Dobyns WB
  Title
De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome.
  Journal
Nat Genet 44:440-4, S1-2 (2012)
DOI:10.1038/ng.1091
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