All diseases

OMIM ID
610798
OMIM term:
IMMUNODEFICIENCY DUE TO DEFECT IN MAPBP-INTERACTING PROTEIN
Alternative terms:

(∗) Location:
1q22  
(†) Associated OMIM genes:
MAPBP-INTERACTING PROTEIN  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/zg7vbe8m