G2Cdb::Human Disease report

Disease id
D00000224
Name
Retinitis pigmentosa
Nervous system disease
no

Genes (1)

Gene Name/Description Mutations Found Literature Mutations Type Genetic association?
G00002481 PRKCG
protein kinase C, gamma
Y (10441600) No mutation found (N) N

References

  • No mutations in the coding region of the PRKCG gene in three families with retinitis pigmentosa linked to the RP11 locus on chromosome 19q.

    Dryja TP, McEvoy J, McGee TL and Berson EL

    Funded by: NEI NIH HHS: EY00169, EY08683, EY11655

    American journal of human genetics 1999;65;3;926-8

Literature (1)

Pubmed - other

  • No mutations in the coding region of the PRKCG gene in three families with retinitis pigmentosa linked to the RP11 locus on chromosome 19q.

    Dryja TP, McEvoy J, McGee TL and Berson EL

    Funded by: NEI NIH HHS: EY00169, EY08683, EY11655

    American journal of human genetics 1999;65;3;926-8

© 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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