reduction of neutrophil motility Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal reduction of the cell motility of neutrophils. (Human Phenotype Ontology, HP_0005400)
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1 genes associated with the reduction of neutrophil motility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
SLC35C1 solute carrier family 35 (GDP-fucose transporter), member C1