All diseases

OMIM ID
303600
OMIM term:
COFFIN-LOWRY SYNDROME; CLS
Alternative terms:

(∗) Location:
Xp22.12  
(†) Associated OMIM genes:
RPS6KA3  
(‡) Associated MGI genes:
Rps6ka3  

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/j5h4pv1h