All diseases

OMIM ID
244200
OMIM term:
KALLMANN SYNDROME 3; KAL3
Alternative terms:

(∗) Location:
20p12.3  
(†) Associated OMIM genes:
PROKR2  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/88ana6fi