Symbol Name ID |
Ncf1
neutrophil cytosolic factor 1 MGI:97283 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Abnormality of neutrophils |
Impaired oxidative burst |
Granulomatosis |
Splenomegaly |
Disease(s) Associated with NCF1 | ||||
autosomal recessive chronic granulomatous disease 1 | ||||
chronic granulomatous disease |
Mouse Phenotypes | hematopoietic system phenotype |
enlarged spleen |
abnormal spleen morphology |
abnormal neutrophil physiology |
impaired granulocyte bactericidal activity |
abnormal macrophage physiology |
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Availability | Mouse Genotype | ||||||
Ncf1em1(IMPC)Mbp/Ncf1em1(IMPC)Mbp | |||||||
Ncf1em1Nansh/Ncf1em1Nansh | * | ||||||
Ncf1m1J/Ncf1m1J | |||||||
Ncf1tm1Hbd/Ncf1tm1Hbd |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 05/28/2024 MGI 6.13 |
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