" /> NCF1 wt Allele - CISMeF





Preferred Label : NCF1 wt Allele;

NCIt synonyms : SH3PXD1A; p47 phox; NOXO2; Chronic Granulomatous Disease, Autosomal 1 Gene; p47-phox; Neutrophil Cytosolic Factor 1, (Chronic Granulomatous Disease, Autosomal 1) Gene; CGD1; p47phox; Neutrophil Cytosolic Factor 1 (47kD, Chronic Granulomatous Disease, Autosomal 1) Gene; Neutrophil Cytosolic Factor 1 wt Allele; NCF1A;

NCIt definition : Human NCF1 wild-type allele is located in the vicinity of 7q11.23 and is approximately 15 kb in length. This allele, which encodes neutrophil cytosol factor 1 protein, plays a role in the regulation of the phagosomal oxidative burst. Mutation of the gene is associated with autosomal recessive chronic granulomatous disease type 1.;

NCI Metathesaurus CUI : CL1662248;

GenBank Accession Number : M25665;

Details


You can consult :


Nous contacter.
04/05/2025


[Home] [Top]

© Rouen University Hospital. Any partial or total use of this material must mention the source.