G2Cdb::Allele report

Mutation type
N

Altered genes (1)

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

Diseases (1)

Disease Description Nervous effect
D00000224 Retinitis pigmentosa 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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