All diseases

OMIM ID
607681
OMIM term:
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2; ECA2
Alternative terms:

(∗) Location:
5q34  
(†) Associated OMIM genes:
GABRG2  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/wd74duxa