TEX14

testis expressed 14, intercellular bridge forming factor

Summary

The protein encoded by this gene is necessary for intercellular bridges in germ cells, which are required for spermatogenesis. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jan 2011]

Known Variants139 total

rsidPosition (GRCh37)AllelesClassClinVar
rs53882827417:56,634,404T/C—uncertain significance
rs77806833817:56,635,178C/A—uncertain significance
rs722512817:56,636,854T/C—benign
rs990305017:56,636,908T/C—benign
rs14757560917:56,636,922C/T—uncertain significance
rs37013662617:56,636,933C/T—likely benign
rs11456265717:56,638,900G/A—likely benign
rs36792863817:56,638,915C/T—likely benign
rs138702256917:56,638,932T/G—uncertain significance
rs735950117:56,641,200C/Tintron variant—
rs15038517217:56,642,242T/C—uncertain significance
rs3481846717:56,643,109A/G—benign
rs75400365517:56,643,165C/A—uncertain significance
rs78049323817:56,646,597A/G—uncertain significance
rs14564363017:56,646,615G/A—uncertain significance
rs5575991217:56,646,622C/T—conflicting classifications of pathogenicity
rs19236920717:56,649,275T/C—likely benign
rs14153129717:56,649,302G/A—uncertain significance
rs15089669917:56,649,334A/G—uncertain significance
rs204454195817:56,649,340T/C—uncertain significance
rs135550732917:56,649,347T/A—likely pathogenic
rs250949287617:56,649,373G/C—uncertain significance
rs214436321117:56,649,450G/T—pathogenic
rs75331661217:56,650,578G/A—uncertain significance
rs77755377717:56,650,579G/T—uncertain significance
rs14715023417:56,650,586T/G—uncertain significance
rs37537835317:56,650,629C/G—uncertain significance
rs36795198117:56,650,631T/C—uncertain significance
rs77614222717:56,650,650C/A—uncertain significance
rs5576854717:56,650,660C/T—likely benign
rs76516638717:56,650,661G/A—uncertain significance
rs124234426817:56,654,751A/C—uncertain significance
rs14844617817:56,654,760C/T—likely benign
rs133125988517:56,657,084A/C—uncertain significance
rs19392079617:56,659,000G/A—uncertain significance
rs650387017:56,659,018C/T—benign
rs11577079017:56,659,019C/T—uncertain significance
rs250950906817:56,659,036T/G—uncertain significance
rs77580189017:56,659,082T/C—likely benign
rs5631533717:56,661,864G/T—pathogenic
rs76065753017:56,661,902C/T—uncertain significance
rs36929227217:56,663,270G/A—uncertain significance
rs214441238917:56,663,288G/A—pathogenic
rs5592499917:56,663,295C/A—benign
rs20108632517:56,663,333C/T—uncertain significance
rs204496015517:56,663,339G/T—uncertain significance
rs75989007717:56,663,354C/T—uncertain significance
rs126048258817:56,663,355G/A—likely benign
rs5634345117:56,663,450A/G—benign
rs77978729417:56,665,290G/A—uncertain significance
rs74640310717:56,670,938T/C—uncertain significance
rs75941678717:56,671,018G/A—likely benign
rs117797932217:56,676,244G/C—uncertain significance
rs14868553617:56,676,258G/A—likely benign
rs250953474817:56,676,259G/A—uncertain significance
rs90268429517:56,676,281C/G—uncertain significance
rs11414584417:56,676,283G/A—likely benign
rs78027293817:56,676,293C/A—uncertain significance
rs11672413517:56,676,322T/C—uncertain significance
rs250953488317:56,676,341C/T—uncertain significance
rs38938917:56,676,368T/C—benign
rs156772673117:56,676,379C/G—uncertain significance
rs20204334217:56,676,398A/G—uncertain significance
rs20221964317:56,676,403C/T—conflicting classifications of pathogenicity
rs78167811917:56,676,404G/A—uncertain significance
rs77799642317:56,676,421T/C—uncertain significance
rs15045455417:56,676,488T/C—likely benign
rs14689447617:56,676,544G/A—likely benign
rs94693204117:56,676,629A/G—uncertain significance
rs128659953317:56,676,641A/G—uncertain significance
rs204536908217:56,676,646T/G—uncertain significance
rs14346773717:56,676,727A/G—uncertain significance
rs7903352717:56,676,728T/C—uncertain significance
rs77887701817:56,676,767C/T—uncertain significance
rs134217972117:56,676,781G/C—uncertain significance
rs123692931317:56,676,836C/T—uncertain significance
rs250953584717:56,676,857G/T—uncertain significance
rs204537683317:56,676,869C/T—uncertain significance
rs250953593217:56,676,897C/T—uncertain significance
rs134229203117:56,676,904G/A—uncertain significance
rs77108737717:56,679,182C/T—uncertain significance
rs77597194517:56,679,235T/C—likely benign
rs145829177517:56,679,292T/C—uncertain significance
rs74642367517:56,679,307C/A—uncertain significance
rs13941648717:56,679,798A/G—likely pathogenic
rs76215543717:56,679,803C/G—uncertain significance
rs3496086917:56,679,904C/A—benign
rs118929608017:56,679,907C/T—likely benign
rs76323502217:56,679,925C/T—uncertain significance
rs14795443317:56,682,353T/C—uncertain significance
rs125528121917:56,682,377A/G—uncertain significance
rs14968055417:56,682,405G/C—uncertain significance
rs13794694417:56,682,424G/A—likely benign
rs78045676217:56,682,426C/T—uncertain significance
rs14306593917:56,682,458C/G—uncertain significance
rs74790522517:56,682,490G/A—likely benign
rs37410575717:56,682,495G/A—likely benign
rs30284917:56,685,518C/T——
rs250955427217:56,688,529A/G—likely benign
rs76169106917:56,688,555G/A—uncertain significance

Showing 100 of 139 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.