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Human Disease and Mouse Model Detail
Human Disease Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II
OMIM ID: 233710
Synonyms Cgd, Autosomal Recessive Cytochrome B-Positive, Type II; Granulomatous Disease, Chronic; Granulomatous Disease, Chronic, Due to NCF2 Deficiency; Ncf2, Deficiency of; Neutrophil Cytosol Factor 2, Deficiency of; P67-Phox, Deficiency of
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Ncf2 NCF2*   1:1 Homology

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/09/2014
MGI 5.20
The Jackson Laboratory