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 - other