TEX15 Chromosome 8

Testis expressed 15, meiosis and synapsis associated
26 variants 26 Health Risk

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What This Gene Does
This gene encodes a protein that is required for DNA double-strand break repair, chromosome synapsis, and meiotic recombination in spermatocytes. Male mice with a knockout of the orthologous gene are viable but sterile. Loss-of-function mutations in the orthologous mouse gene cause early meiotic arrest in spermatocytes, before the mid-pachytene stage. Naturally occurring mutations in this gene are associated with nonobstructive azoospermia. [provided by RefSeq, Apr 2017]
Associated Conditions (4)
Spermatogenic failure 25
TEX15-related disorder
Non-obstructive azoospermia
Oligosynaptic infertility
Key Variants
All Variants (26)
RSID Category Clinical Significance Conditions
RS117788795 Health Risk Conflicting classifications of pathogenicity Spermatogenic failure 25, TEX15-related disorder, Spermatogenic failure 25
RS144234582 Health Risk Conflicting classifications of pathogenicity Spermatogenic failure 25, Spermatogenic failure 25
RS145215857 Health Risk Conflicting classifications of pathogenicity Spermatogenic failure 25, Spermatogenic failure 25
RS146619272 Health Risk Conflicting classifications of pathogenicity Spermatogenic failure 25, Spermatogenic failure 25
RS146850714 Health Risk Conflicting classifications of pathogenicity Spermatogenic failure 25, Spermatogenic failure 25
RS150606321 Health Risk Conflicting classifications of pathogenicity Non-obstructive azoospermia, Non-obstructive azoospermia
RS199659098 Health Risk Conflicting classifications of pathogenicity Spermatogenic failure 25, Spermatogenic failure 25
RS376683373 Health Risk Conflicting classifications of pathogenicity Spermatogenic failure 25, Spermatogenic failure 25
RS550195743 Health Risk Conflicting classifications of pathogenicity Spermatogenic failure 25, Spermatogenic failure 25
RS565708396 Health Risk Conflicting classifications of pathogenicity
RS76147771 Health Risk Conflicting classifications of pathogenicity Spermatogenic failure 25, Spermatogenic failure 25
RS767325029 Health Risk Conflicting classifications of pathogenicity Spermatogenic failure 25, Spermatogenic failure 25
RS1224137237 Health Risk Likely pathogenic Spermatogenic failure 25, Spermatogenic failure 25
RS2486836794 Health Risk Likely pathogenic Spermatogenic failure 25, Spermatogenic failure 25
RS752501149 Health Risk Likely pathogenic Spermatogenic failure 25, Spermatogenic failure 25
RS754041709 Health Risk Likely pathogenic Spermatogenic failure 25, Spermatogenic failure 25
RS1244093431 Health Risk Pathogenic Spermatogenic failure 25, Spermatogenic failure 25
RS1351772557 Health Risk Pathogenic Non-obstructive azoospermia, Non-obstructive azoospermia
RS1554491783 Health Risk Pathogenic Spermatogenic failure 25, Spermatogenic failure 25
RS1554492164 Health Risk Pathogenic Spermatogenic failure 25, Spermatogenic failure 25
RS751384082 Health Risk Pathogenic
RS762458625 Health Risk Pathogenic
RS763654373 Health Risk Pathogenic Spermatogenic failure 25, Spermatogenic failure 25
RS864309485 Health Risk Pathogenic Oligosynaptic infertility, Spermatogenic failure 25, Oligosynaptic infertility
RS141978088 Health Risk Pathogenic/Likely pathogenic Spermatogenic failure 25, Spermatogenic failure 25
RS62000447 Health Risk Pathogenic/Likely pathogenic Spermatogenic failure 25, Spermatogenic failure 25
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