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/Guncertain significance
rs250589724115:56,665,662C/Guncertain significance
rs211418315:56,674,892T/Aintron variant
rs3549716715:56,675,814T/A
rs74817317715:56,676,156C/Tuncertain significance
rs14743315915:56,676,171T/Cuncertain significance
rs75231608115:56,676,178C/Guncertain significance
rs254847061315:56,680,710G/Auncertain significance
rs20029645415:56,681,557C/Auncertain significance
rs254847993115:56,683,460G/Auncertain significance
rs11295196815:56,683,478G/Auncertain significance
rs254848040015:56,683,542G/Auncertain significance
rs37324894715:56,683,593G/Auncertain significance
rs136958752015:56,683,604G/Cuncertain significance
rs11742153115:56,693,828A/T
rs37569944915:56,704,607G/Tuncertain significance
rs500538915:56,718,824T/Cdownstream gene variant
rs20197361215:56,719,803G/Tuncertain significance
rs254858037115:56,719,930G/Cuncertain significance
rs254858332815:56,720,586A/Guncertain significance
rs254858348915:56,720,610T/Auncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.