Neutrophil cytosolic factor 1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Neutrophil cytosolic factor 1

Neutrophil cytosol factor 1, also known as p47phox, is a protein that in humans is encoded by the NCF1 gene.[5]

Quick Facts NCF1, Available structures ...
NCF1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesNCF1, NCF1A, NOXO2, SH3PXD1A, p47phox, Neutrophil cytosolic factor 1, CGD1
External IDsOMIM: 608512; MGI: 97283; HomoloGene: 30964; GeneCards: NCF1; OMA:NCF1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000265

NM_001286037
NM_010876

RefSeq (protein)

NP_000256

NP_001272966
NP_035006

Location (UCSC)Chr 7: 74.77 – 74.79 MbChr 5: 134.25 – 134.26 Mb
PubMed search[3][4]
Wikidata
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Function

The protein encoded by this gene is a 47 kDa cytosolic subunit of neutrophil NADPH oxidase. This oxidase is a multicomponent enzyme that is activated to produce superoxide anion. Mutations in this gene have been associated with chronic granulomatous disease.[5]

Genetic variability in the NCF1 gene has been found to be related to a higher chance of getting autoimmune diseases such as Sjögren's syndrome, rheumatoid arthritis and lupus erythematosus.[6]

p47 is vital to the activation of NADPH oxidase. P47 becomes heavily phosphorylated

Interactions

Neutrophil cytosolic factor 1 has been shown to interact with:

References

Further reading

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