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Human Disease and Mouse Model Detail
Human Disease Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I
OMIM ID: 233700
Synonyms Cgd, Autosomal Recessive Cytochrome B-Positive, Type I; Granulomatous Disease, Chronic, Due to NCF1 Deficiency; Ncf1, Deficiency of; Neutrophil Cytosol Factor 1, Deficiency of; P47-Phox, Deficiency of; SOC2, Deficiency of; Soluble Oxidase Component II, Deficiency of
View all models View ALL (4) mouse models for this human disease.
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
     Ncf1* NCF1* View 4 models 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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Send questions and comments to User Support. 		last database update
06/05/2013
MGI 5.13 		The Jackson Laboratory