Search results for: PRKCG

Disease (8)

Disease Description Nervous effect
D00000121 Chronic nonspherocytic haemolytic anaemia N
D00000122 Pyruvate kinase deficiency N
D00000125 Haemolytic anaemia N
D00000185 Cerebellar ataxia (autosomal dominant) Y
D00000186 Cerebellar ataxia (dominant non-episodic) Y
D00000190 Spinocerebellar ataxia type 14 Y
D00000224 Retinitis pigmentosa N
D00000300 Peutz-Jeghers syndrome N

Gene (1)

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