G2Cdb::Allele report

Mutation type
MI

Altered genes (1)

Gene Symbol Species Description
G00002481 PRKCG Homo sapiens protein kinase C, gamma

Diseases (1)

Disease Description Nervous effect
D00000190 Spinocerebellar ataxia type 14 Y

Literature (1)

Pubmed - human_disease

© 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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