All diseases

OMIM ID
217095
OMIM term:
CONOTRUNCAL HEART MALFORMATIONS; CTHM TRUNCUS ARTERIOSUS COMMUNIS, INCLUDED
Alternative terms:
CONOTRUNCAL ANOMALY FACE SYNDROME, INCLUDED; CAFS, INCLUDED
DOUBLE-OUTLET RIGHT VENTRICLE, INCLUDED; DORV, INCLUDED
PERSISTENT TRUNCUS ARTERIOSUS, INCLUDED; PTA, INCLUDED
INTERRUPTED AORTIC ARCH, INCLUDED
(∗) Location:
18q11.2   19p13.11   22q11.21   2q21.1   5q35.1   8p21.2  
(†) Associated OMIM genes:
CFC1   GATA6   GDF1   NKX2-5   NKX2-6   TBX1  
(‡) Associated MGI genes:
Cfc1   Ece1  

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/occm3330