All diseases

OMIM ID
602481
OMIM term:
MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2
Alternative terms:

(∗) Location:
1q23.2  
(†) Associated OMIM genes:
ATP1A2  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/wxg0z6b8