G2Cdb::Allele report

Mutation type
MI

Altered genes (1)

Gene Symbol Species Description
G00002000 MYO5A Homo sapiens myosin VA (heavy chain 12, myoxin)

Diseases (1)

Disease Description Nervous effect
D00000135 Griscelli syndrome N

Literature (1)

Pubmed - other

© G2C 2014. The Genes to Cognition Programme received funding from The Wellcome Trust and the EU FP7 Framework Programmes:
EUROSPIN (FP7-HEALTH-241498), SynSys (FP7-HEALTH-242167) and GENCODYS (FP7-HEALTH-241995).

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