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