MYPOP

Myb related transcription factor, partner of profilin

Summary

Predicted to enable DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants33 total

rsidPosition (GRCh37)AllelesClassClinVar
rs128043478019:46,393,963A/Guncertain significance
rs76483278719:46,393,972G/Tuncertain significance
rs75290540719:46,393,978G/Auncertain significance
rs139566316119:46,393,981C/Tuncertain significance
rs77776469219:46,393,982G/Auncertain significance
rs74582026219:46,393,987G/Tuncertain significance
rs148059519319:46,394,011A/Cuncertain significance
rs76358131719:46,394,042C/Guncertain significance
rs53183948619:46,394,063C/Tuncertain significance
rs251382264419:46,394,179G/Tuncertain significance
rs55873278819:46,394,249C/Tuncertain significance
rs37239611819:46,394,260C/Tuncertain significance
rs104430756419:46,394,290C/Tuncertain significance
rs11438760219:46,394,322G/Asynonymous variant
rs76537800819:46,394,329G/Cuncertain significance
rs75267274419:46,394,347G/Auncertain significance
rs20101890819:46,394,468G/Cuncertain significance
rs37355948919:46,394,483G/Cuncertain significance
rs20170773819:46,394,533G/Cuncertain significance
rs1297665219:46,396,610T/Cintron variant
rs7548077419:46,397,887T/Cintron variant
rs7436934119:46,397,888T/Gintron variant
rs3493436019:46,398,989A/Gregulatory region variant
rs77218776619:46,404,554G/Tuncertain significance
rs251383191419:46,404,557C/Auncertain significance
rs75841949319:46,404,617C/Tuncertain significance
rs140300267719:46,404,709G/Auncertain significance
rs75499726519:46,404,752C/Tuncertain significance
rs160057345519:46,404,779G/Auncertain significance
rs251383243019:46,404,783G/Tuncertain significance
rs141189672319:46,404,860C/Tuncertain significance
rs75715078719:46,404,923G/Auncertain significance
rs53080073919:46,405,010C/Tuncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.