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 |
|---|---|---|
| D00000185 | Cerebellar ataxia (autosomal dominant) | Y |
© 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).
EUROSPIN (FP7-HEALTH-241498), SynSys (FP7-HEALTH-242167) and GENCODYS (FP7-HEALTH-241995).