All diseases

OMIM ID
600059
OMIM term:
RETINITIS PIGMENTOSA 13; RP13
Alternative terms:

(∗) Location:
17p13.3  
(†) Associated OMIM genes:
PRPF8  
(‡) Associated MGI genes:
Prpf8  

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/u7blzwvj