azoospermia Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A male infertility disease characterized by the absence of any measurable level of sperm in semen. (Human Disease Ontology, DOID_14227)
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24 genes associated with the disease azoospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
AR androgen receptor
ART3 ADP-ribosyltransferase 3
BCL2 B-cell CLL/lymphoma 2
BRD2 bromodomain containing 2
CDK2 cyclin-dependent kinase 2
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
ERCC1 excision repair cross-complementation group 1
ERCC2 excision repair cross-complementation group 2
FKBP6 FK506 binding protein 6, 36kDa
FSHR follicle stimulating hormone receptor
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HLA-DRA major histocompatibility complex, class II, DR alpha
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
IL1B interleukin 1, beta
PATZ1 POZ (BTB) and AT hook containing zinc finger 1
PRDM9 PR domain containing 9
PSMC3IP PSMC3 interacting protein
SOHLH1 spermatogenesis and oogenesis specific basic helix-loop-helix 1
SOX5 SRY (sex determining region Y)-box 5
SYCP3 synaptonemal complex protein 3
UBE2B ubiquitin-conjugating enzyme E2B
VPS52 vacuolar protein sorting 52 homolog (S. cerevisiae)
XRCC1 X-ray repair complementing defective repair in Chinese hamster cells 1
ZNF230 zinc finger protein 230