reduced sperm motility Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal reduction in the mobility of ejaculated sperm. (Human Phenotype Ontology, HP_0012207)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012207
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Genes

3 genes associated with the reduced sperm motility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
C21ORF59 chromosome 21 open reading frame 59
CATSPER1 cation channel, sperm associated 1
ZMYND10 zinc finger, MYND-type containing 10