abnormal spermatogenesis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Incomplete maturation or aberrant formation of the male gametes. (Human Phenotype Ontology, HP_0008669)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008669
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17 genes associated with the abnormal spermatogenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AR androgen receptor
ATM ATM serine/threonine kinase
BLM Bloom syndrome, RecQ helicase-like
CATSPER1 cation channel, sperm associated 1
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CNBP CCHC-type zinc finger, nucleic acid binding protein
DAZ1 deleted in azoospermia 1
HFE hemochromatosis
NANOS1 nanos homolog 1 (Drosophila)
NR5A1 nuclear receptor subfamily 5, group A, member 1
POC1A POC1 centriolar protein A
SCP2 sterol carrier protein 2
STEAP3 STEAP family member 3, metalloreductase
SYCP3 synaptonemal complex protein 3
TAF4B TAF4b RNA polymerase II, TATA box binding protein (TBP)-associated factor, 105kDa
USP9Y ubiquitin specific peptidase 9, Y-linked
ZMYND15 zinc finger, MYND-type containing 15