Search results for: MYO5A

Disease (10)

Disease Description Nervous effect
D00000093 Acute myeloid leukaemia N
D00000132 Macrothrombocytopenia (autosomal dominant) N
D00000135 Griscelli syndrome N
D00000136 Griscelli syndrome type 3 N
D00000166 Schizophrenia Y
D00000182 Encephalomyopathy N
D00000208 Myopathy (autosomal dominant) N
D00000235 Hypertrophic cardiomyopathy N
D00000236 Hypertrophic cardiomyopathy (familial) N
D00000237 Idiopathic dilated cardiomyopathy N

Gene (2)

Gene Symbol Species Description
G00000751 Myo5a Mus musculus myosin VA
G00002000 MYO5A Homo sapiens myosin VA (heavy chain 12, myoxin)
© 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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