All diseases

OMIM ID
606056
OMIM term:
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIb; CDG2B
Alternative terms:
CDG IIb; CDGIIb
GLUCOSIDASE I DEFICIENCY
(∗) Location:
2p13.1  
(†) Associated OMIM genes:
GCS1  
(‡) 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/kot9efho