All diseases

OMIM ID
612287
OMIM term:
NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 2; NPHLOP2
Alternative terms:

(∗) Location:
17q25.1  
(†) Associated OMIM genes:
SLC9A3R1  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/bp4yyvn7