All diseases

OMIM ID
300534
OMIM term:
MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ
Alternative terms:

(∗) Location:
Xp11.22  
(†) Associated OMIM genes:
KDM5C  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/rt0mg8my