G2Cdb::Human Disease report

Disease id
D00000190
Name
Spinocerebellar ataxia type 14
Nervous system disease
yes

Genes (1)

Gene Name/Description Mutations Found Literature Mutations Type Genetic association?
G00002481 PRKCG
protein kinase C, gamma
Y (15313841) Single nucleotide polymorphism (SNP) Y
G00002481 PRKCG
protein kinase C, gamma
Y (14676051) Microinsertion (MI) Y
G00002481 PRKCG
protein kinase C, gamma
Y (16189624) Microinsertion (MI) Y

References

Literature (3)

Pubmed - human_disease

Pubmed - other

© 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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