All diseases

OMIM ID
248250
OMIM term:
HYPOMAGNESEMIA 3, RENAL; HOMG3
Alternative terms:
HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORT OF MAGNESIUM
HYPOMAGNESEMIA, ISOLATED RENAL
HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS HYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED
(∗) Location:
3q28  
(†) Associated OMIM genes:
CLDN16  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/33h8jdo9