All diseases

OMIM ID
300497
OMIM term:
ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2; ASPGX2
Alternative terms:

(∗) Location:
Xp22.32-p22.31  
(†) Associated OMIM genes:
NLGN4  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/1ztw3tk4