TMEM260

transmembrane protein 260

Summary

Enables dolichyl-phosphate-mannose-protein mannosyltransferase activity. Involved in protein maturation. Is active in endoplasmic reticulum membrane. Implicated in T-cell non-Hodgkin lymphoma; non-Hodgkin lymphoma; and stomach cancer. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants98 total

rsidPosition (GRCh37)AllelesClassClinVar
rs53469189114:57,046,665C/T—likely benign
rs54664647514:57,046,691T/C—likely benign
rs56806035814:57,046,707C/T—conflicting classifications of pathogenicity
rs188500114014:57,046,723G/C—uncertain significance
rs37680067514:57,046,735G/A—uncertain significance
rs55764588614:57,046,739T/C—uncertain significance
rs57580371814:57,046,748T/A—uncertain significance
rs74624708014:57,046,765C/T—uncertain significance
rs20105958714:57,046,768C/A—benign
rs122325043214:57,046,790C/T—uncertain significance
rs159479913814:57,046,799T/A—likely benign
rs188545508914:57,052,477A/G—pathogenic
rs77190125414:57,052,491C/G—uncertain significance
rs75998190014:57,052,523A/T—uncertain significance
rs188546038414:57,052,527G/A—uncertain significance
rs6173266514:57,052,547T/C—benign
rs74562060314:57,052,554A/G—likely benign
rs37681803214:57,052,570A/G—uncertain significance
rs76788004214:57,052,585T/C—uncertain significance
rs74763268614:57,052,630G/A—pathogenic
rs1078243314:57,070,501A/G—benign
rs144783365214:57,070,565C/T—uncertain significance
rs14970596514:57,070,588C/T—uncertain significance
rs14545586414:57,070,589G/A—uncertain significance
rs14665499814:57,070,596A/T—likely benign
rs96596432514:57,070,661C/T—uncertain significance
rs188684487514:57,072,294A/G—uncertain significance
rs75811399414:57,072,307T/G—uncertain significance
rs77964168114:57,072,310G/A—uncertain significance
rs76178556814:57,072,342A/G—uncertain significance
rs75112929614:57,072,369C/T—uncertain significance
rs122356015114:57,072,370C/G—uncertain significance
rs15043923314:57,075,836G/C—uncertain significance
rs6173270214:57,075,855G/T—conflicting classifications of pathogenicity
rs250353418514:57,075,863T/G—uncertain significance
rs14956933614:57,075,872G/A—uncertain significance
rs250353428914:57,075,881C/T—uncertain significance
rs36910645414:57,075,896C/A—uncertain significance
rs76035098014:57,075,917C/T—uncertain significance
rs1777625614:57,075,920G/T—likely pathogenic
rs56488108114:57,075,924G/A—uncertain significance
rs20036000314:57,075,939A/T—uncertain significance
rs1013779914:57,075,976C/T—benign
rs74659054414:57,078,954T/A—uncertain significance
rs227502414:57,082,648G/A—benign
rs14857060014:57,082,668A/G—uncertain significance
rs75491839714:57,082,682G/A—likely benign
rs77252196414:57,083,914C/G—uncertain significance
rs74871356714:57,083,957C/T—uncertain significance
rs213959177014:57,085,325G/A—pathogenic
rs159485575314:57,085,347G/T—likely benign
rs250357509614:57,085,391C/A—uncertain significance
rs74601853214:57,085,448T/C—uncertain significance
rs37627641114:57,085,480A/G—uncertain significance
rs142194901114:57,085,490T/C—likely benign
rs75919029314:57,088,249T/C—likely benign
rs75689589314:57,088,254G/C—uncertain significance
rs116511657414:57,088,288C/G—uncertain significance
rs20195646914:57,088,415C/Tstop gainedpathogenic
rs37547646314:57,092,111C/A—pathogenic
rs11327763714:57,092,112G/A—likely benign
rs18234036914:57,092,142T/C—likely benign
rs75031940914:57,092,167A/C—uncertain significance
rs37160107614:57,092,169C/T—uncertain significance
rs156656143914:57,092,173G/A—likely pathogenic
rs37643523514:57,092,190A/G—uncertain significance
rs37232158014:57,099,751A/G—uncertain significance
rs13908953414:57,099,820T/C—uncertain significance
rs76020691514:57,099,836G/C—uncertain significance
rs104131614:57,099,859G/A—benign
rs20072981114:57,099,860T/C—likely benign
rs120410157814:57,099,889G/T—uncertain significance
rs76144311214:57,101,636G/C—likely pathogenic
rs54906550614:57,101,656A/G—likely benign
rs91374214:57,101,682A/G—benign
rs7780260714:57,103,222C/G—benign
rs37085242314:57,103,228T/C—uncertain significance
rs20170525714:57,103,237C/T—uncertain significance
rs14841813314:57,103,263A/T—uncertain significance
rs147791463514:57,103,287A/G—uncertain significance
rs14642237514:57,103,301C/T—likely benign
rs15122885814:57,103,316C/T—likely benign
rs14159909214:57,103,317G/T—likely pathogenic
rs6173940714:57,113,980A/G—uncertain significance
rs146426125414:57,113,997C/A—uncertain significance
rs14916472814:57,114,018T/C—uncertain significance
rs13901919214:57,114,027G/A—uncertain significance
rs76153679114:57,114,045C/T—uncertain significance
rs14704224914:57,114,085C/T—uncertain significance
rs56185136014:57,114,100A/G—uncertain significance
rs36955639114:57,114,105C/T—uncertain significance
rs250370235414:57,114,121A/C—uncertain significance
rs76952933214:57,114,127C/T—likely benign
rs76548872614:57,114,192C/G—uncertain significance
rs15065476914:57,114,193T/C—uncertain significance
rs75500928214:57,114,203G/A—likely benign
rs490170614:57,114,385G/T——
rs75331227614:57,127,937G/T——

Gene information from NCBI Gene. Variant classifications from ClinVar.