All diseases

OMIM ID
610725
OMIM term:
NEPHROTIC SYNDROME, TYPE 3; NPHS3
Alternative terms:

(∗) Location:
10q23.33  
(†) Associated OMIM genes:
PLCE1  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/01bgaxaj