All diseases

OMIM ID
606170
OMIM term:
GENITOPATELLAR SYNDROME; GTPTS
Alternative terms:

(∗) Location:
10q22.2  
(†) Associated OMIM genes:
KAT6B  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/1v4o4inr