All diseases

OMIM ID
611131
OMIM term:
RETINITIS PIGMENTOSA 37; RP37
Alternative terms:

(∗) Location:
15q23  
(†) Associated OMIM genes:
NR2E3  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/lld9m90p