| Name: neutrophil cytosolic factor 1 |
| Aliases:
p47phox,
NADPH oxidase subunit (47kDa),
p47<phox>,
Ncf-1,
NOXO2,
meutrophil cytosolic factor 1
|
| Description: PHENOTYPE: Homozygous disruption of this gene causes severe spontaneous infections and granulomatous inflammation and may alter synaptic plasticity and memory, RAS activation, blood pressure control, airway smooth muscle function, neointima formation, vasoconstriction and the response to myocardial infarction. [provided by MGI curators] |
| Crossreferences:
MGI:97283,
UniProtKB:Q7TMH0,
UniProtKB:Q3UA02,
UniProtKB:Q3U9Y3,
UniProtKB:S4R293,
UniProtKB:Q09014,
UniProtKB:F8WH69,
ENSEMBL:ENSMUSG00000015950,
NCBI_Gene:17969,
UniProtKB:Q3UBI5
|
| This information is supplied by the AllianceGenome.org API. |