All diseases

OMIM ID
268000
OMIM term:
RETINITIS PIGMENTOSA; RP
Alternative terms:

(∗) Location:
14q31.3  
(†) Associated OMIM genes:
SPATA7  
(‡) Associated MGI genes:
Ccdc66   Cngb1   Pde6a   Pde6b   Pde6g   Prph2   Rho   Slc6a6  

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/qf78foe3