All diseases

OMIM ID
312600
OMIM term:
RETINITIS PIGMENTOSA 2; RP2
Alternative terms:

(∗) Location:
Xp11.23  
(†) Associated OMIM genes:
RP2  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/x1zkyre8