All diseases

OMIM ID
608454
OMIM term:
KNOBLOCH SYNDROME 2; KNO2
Alternative terms:

(∗) Location:
16q23.1  
(†) Associated OMIM genes:
ADAMTS18  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/lsvp0soe