All diseases

OMIM ID
201000
OMIM term:
CARPENTER SYNDROME
Alternative terms:
ACROCEPHALOPOLYSYNDACTYLY TYPE II
ACPS II
(∗) Location:
6p11.2  
(†) Associated OMIM genes:
RAB23  
(‡) 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/iz521kfu