non-obstructive azoospermia Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Absence of any measurable level of sperm in his semen, resulting from a defect in the production of spermatozoa in the testes. Can be differentiated from obstructive azoospermia on the basis of testicular biopsy. (Human Phenotype Ontology, HP_0011961)
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26 genes associated with the non-obstructive azoospermia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
PTK2 protein tyrosine kinase 2 1.63966
CHSY1 chondroitin sulfate synthase 1 1.61479
CFB complement factor B 1.56721
HLA-DRA major histocompatibility complex, class II, DR alpha 1.56375
TDRKH tudor and KH domain containing 1.51446
C6ORF10 chromosome 6 open reading frame 10 1.49433
FAT1 FAT atypical cadherin 1 1.47064
FAM155A family with sequence similarity 155, member A 1.39047
BTNL2 butyrophilin-like 2 1.35521
MOBP myelin-associated oligodendrocyte basic protein 1.34987
SOX5 SRY (sex determining region Y)-box 5 1.32793
LOC100289473 cytoskeleton associated protein 2-like pseudogene 1.32793
PTPRD protein tyrosine phosphatase, receptor type, D 1.19288
GALNT12 polypeptide N-acetylgalactosaminyltransferase 12 1.15698
SLCO5A1 solute carrier organic anion transporter family, member 5A1 1.13911
MARCO macrophage receptor with collagenous structure 1.04564
ESR2 estrogen receptor 2 (ER beta) 1.03995
ANAPC4 anaphase promoting complex subunit 4 1.02002
ASTN2 astrotactin 2 1.0154
NOTCH4 notch 4 0.964368
AOX2P aldehyde oxidase 2 pseudogene 0.90455
DNAH10 dynein, axonemal, heavy chain 10 0.897419
OR56A4 olfactory receptor, family 56, subfamily A, member 4 0.872126
PHF2P1 PHD finger protein 2 pseudogene 1 0.85862
LHFPL3 lipoma HMGIC fusion partner-like 3 0.808534
TSNARE1 t-SNARE domain containing 1 0.776085