All diseases

OMIM ID
118450
OMIM term:
ALAGILLE SYNDROME 1; ALGS1
Alternative terms:
ALAGILLE SYNDROME; ALGS
ALAGILLE-WATSON SYNDROME; AWS
CHOLESTASIS WITH PERIPHERAL PULMONARY STENOSIS
ARTERIOHEPATIC DYSPLASIA; AHD
HEPATIC DUCTULAR HYPOPLASIA, SYNDROMATIC
(∗) Location:
20p12.2  
(†) Associated OMIM genes:
JAG1  
(‡) Associated MGI genes:
Jag1  

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/jjqfv2u1