abnormality of neutrophil physiology Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A functional abnormality of neutrophils. (Human Phenotype Ontology, HP_0011990)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011990
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Genes

6 genes associated with the abnormality of neutrophil physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CYBA cytochrome b-245, alpha polypeptide
CYBB cytochrome b-245, beta polypeptide
GPI glucose-6-phosphate isomerase
NCF1 neutrophil cytosolic factor 1
NCF2 neutrophil cytosolic factor 2
SLC35C1 solute carrier family 35 (GDP-fucose transporter), member C1