All diseases

OMIM ID
600955
OMIM term:
PROPROTEIN CONVERTASE 1/3 DEFICIENCY
Alternative terms:

(∗) Location:
5q15  
(†) Associated OMIM genes:
PCSK1  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/4n9he726