Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
0.370 Biomarker disease CTD_human Mutant protein kinase C gamma that causes spinocerebellar ataxia type 14 (SCA14) is selectively degraded by autophagy. 20398063 2010
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
0.370 GeneticVariation disease BEFREE Recent observations suggest that the human episodic ataxia 2 (EA2) and spinocerebellar ataxia types 6 (SCA6), 12 (SCA12), and 14 (SCA14) might be associated with impaired phosphorylation levels of cerebellum calcium channels and receptors. 19488825 2009
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
0.370 GeneticVariation disease LHGDN Another mutation in cysteine 131 in protein kinase C gamma as a cause of spinocerebellar ataxia type 14. 17562946 2007
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
0.370 GeneticVariation disease BEFREE This delay was accompanied by stabilization of p300/CBP, transcriptional mediators whose abundance and activity would otherwise decline in the course of the SCA1 disease, and persistence of protein kinase C gamma (PKCgamma), a protein involved in Purkinje cell dendritic development that is mutated in one form of spinocerebellar ataxia. 16409551 2006
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
0.370 GeneticVariation disease BEFREE It has been reported that mutations of gammaPKC cause hereditary spinocerebellar atrophy type 14 (SCA14). 16828200 2006
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
0.370 GeneticVariation disease BEFREE Novel PRKCG/SCA14 mutation in a Dutch spinocerebellar ataxia family: expanding the phenotype. 16547918 2006
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
0.370 GeneticVariation disease LHGDN Mutant protein kinase Cgamma found in spinocerebellar ataxia type 14 is susceptible to aggregation and causes cell death. 15964845 2005
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
0.370 GeneticVariation disease LHGDN Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gamma. 14676051 2003