TEX9

testis expressed 9

Summary

Located in centriolar satellite. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants27 total

rsidPosition (GRCh37)AllelesClassClinVar
rs268205315:56,544,917G/Aintron variant—
rs271393615:56,545,985A/Cintron variant—
rs1163209115:56,548,605C/T——
rs2860455615:56,599,832G/Aintron variant—
rs246540815:56,608,703G/C——
rs716888615:56,624,382G/C——
rs77264561915:56,657,658C/G—uncertain significance
rs250589724115:56,665,662C/G—uncertain significance
rs211418315:56,674,892T/Aintron variant—
rs3549716715:56,675,814T/A——
rs74817317715:56,676,156C/T—uncertain significance
rs14743315915:56,676,171T/C—uncertain significance
rs75231608115:56,676,178C/G—uncertain significance
rs254847061315:56,680,710G/A—uncertain significance
rs20029645415:56,681,557C/A—uncertain significance
rs254847993115:56,683,460G/A—uncertain significance
rs11295196815:56,683,478G/A—uncertain significance
rs254848040015:56,683,542G/A—uncertain significance
rs37324894715:56,683,593G/A—uncertain significance
rs136958752015:56,683,604G/C—uncertain significance
rs11742153115:56,693,828A/T——
rs37569944915:56,704,607G/T—uncertain significance
rs500538915:56,718,824T/Cdownstream gene variant—
rs20197361215:56,719,803G/T—uncertain significance
rs254858037115:56,719,930G/C—uncertain significance
rs254858332815:56,720,586A/G—uncertain significance
rs254858348915:56,720,610T/A—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.