All diseases

OMIM ID
121201
OMIM term:
SEIZURES, BENIGN FAMILIAL NEONATAL, 2; BFNS2
Alternative terms:

(∗) Location:
8q24.22  
(†) Associated OMIM genes:
KCNQ3  
(‡) Associated MGI genes:
Kcnq3  

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/tt4dhxs9