abnormal sperm motility Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly of the mobility of ejaculated sperm. (Human Phenotype Ontology, HP_0012206)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012206
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5 genes associated with the abnormal 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
DNAAF5 dynein, axonemal, assembly factor 5
RSPH9 radial spoke head 9 homolog (Chlamydomonas)
ZMYND10 zinc finger, MYND-type containing 10