All diseases

OMIM ID
176430
OMIM term:
PREMATURE CHROMATID SEPARATION TRAIT; PCS
Alternative terms:

(∗) Location:
15q15.1  
(†) Associated OMIM genes:
BUB1B  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/cshyz0cs