All diseases

OMIM ID
612437
OMIM term:
EPILEPSY, PROGRESSIVE MYOCLONIC 1B; EPM1B
Alternative terms:

(∗) Location:
12q12  
(†) Associated OMIM genes:
PRICKLE1  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/nlv5h3it