All diseases

OMIM ID
610188
OMIM term:
JOUBERT SYNDROME 5; JBTS5
Alternative terms:

(∗) Location:
12q21.32  
(†) Associated OMIM genes:
CEP290  
(‡) Associated MGI genes:
Cep290  

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/m81jjgqt