All diseases

OMIM ID
607872
OMIM term:
CHROMOSOME 1p36 DELETION SYNDROME
Alternative terms:

(∗) Location:
1p36  
(†) Associated OMIM genes:
(‡) Associated MGI genes:
Kcnab2  

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/54f257p3