G2Cdb::Search
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 |