rs4821544

This is a regulatory region variant variant in the NCF4 gene.

GWAS Catalog Trait Associations (4)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

thiosulfate sulfurtransferase measurement

Allele C
OR 0.09
p 1.0e-42
N 47,745
Large GWAS
European

basophil count, eosinophil count

Allele C
OR 0.03
p 5.0e-14
N 171,771
Large GWAS
European

eosinophil count

Allele C
OR 0.03
p 5.0e-13
N 172,275
Large GWAS
European
Allele C
OR 0.02
p 2.0e-8
N 365,954
Large GWAS
European

Crohn's disease

Allele C
OR 1.10
p 2.0e-8
N 40,266
Large GWAS
European, NR

ClinVar annotation

Benign☆☆☆
1 submitter1 publication

Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 3

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About NCF4

The protein encoded by this gene is a cytosolic regulatory component of the superoxide-producing phagocyte NADPH-oxidase, a multicomponent enzyme system important for host defense. This protein is preferentially expressed in cells of myeloid lineage. It interacts primarily with neutrophil cytosolic factor 2 (NCF2/p67-phox) to form a complex with neutrophil cytosolic factor 1 (NCF1/p47-phox), which further interacts with the small G protein RAC1 and translocates to the membrane upon cell stimulation. This complex then activates flavocytochrome b, the membrane-integrated catalytic core of the enzyme system. The PX domain of this protein can bind phospholipid products of the PI(3) kinase, which suggests its role in PI(3) kinase-mediated signaling events. The phosphorylation of this protein was found to negatively regulate the enzyme activity. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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