All diseases

OMIM ID
214150
OMIM term:
CEREBROOCULOFACIOSKELETAL SYNDROME 1; COFS1
Alternative terms:
COFS SYNDROME; COFS
PENA-SHOKEIR SYNDROME, TYPE II
(∗) Location:
10q11.23  
(†) Associated OMIM genes:
ERCC6  
(‡) Associated MGI genes:

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/jd2n0nvm