All diseases

OMIM ID
207750
OMIM term:
APOLIPOPROTEIN C-II DEFICIENCY
Alternative terms:
HYPERLIPOPROTEINEMIA, TYPE IB
C-II ANAPOLIPOPROTEINEMIA
APOC2 DEFICIENCY
(∗) Location:
19q13.32  
(†) Associated OMIM genes:
APOC2  
(‡) 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/elcqz0mo