All diseases

OMIM ID
610498
OMIM term:
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2; COXPD2
Alternative terms:

(∗) Location:
10q22.2  
(†) Associated OMIM genes:
MRPS16  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/ct52xwis