azoospermia Gene Set

Dataset	GAD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A condition of suboptimal concentration of SPERMATOZOA in the ejaculated SEMEN to ensure successful FERTILIZATION of an OVUM. In humans, oligospermia is defined as a sperm count below 20 million per milliliter semen. (Experimental Factor Ontology, EFO_0000279)
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Genes

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