TSHZ2

teashirt zinc finger homeobox 2

Summary

This gene is a member of the teashirt C2H2-type zinc-finger protein family of transcription factors. This gene encodes a protein with five C2H2-type zinc fingers, a homeobox DNA-binding domain and a coiled-coil domain. This nuclear protein is predicted to act as a transcriptional repressor. This gene is thought to play a role in the development and progression of breast and other types of cancer. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]

Known Variants80 total

rsidPosition (GRCh37)AllelesClassClinVar
rs5713942920:51,587,111A/Gupstream gene variant
rs189220320:51,696,096C/Tregulatory region variant
rs274739920:51,707,666G/Aintron variant
rs129343020:51,734,779T/Gintron variant
rs1169685220:51,770,946C/Tintron variant
rs11817408120:51,778,123C/Tregulatory region variant
rs14818803020:51,779,041A/Gregulatory region variant
rs20179905320:51,870,106G/Auncertain significance
rs77672247020:51,870,148G/Auncertain significance
rs77430309420:51,870,155A/Cuncertain significance
rs14693723120:51,870,169C/Tuncertain significance
rs37371208420:51,870,173A/Guncertain significance
rs251604322020:51,870,198G/Cuncertain significance
rs20224685920:51,870,244T/Glikely benign
rs37087114120:51,870,279C/Guncertain significance
rs4544829720:51,870,295G/Auncertain significance
rs251604376520:51,870,301G/Cuncertain significance
rs104374133520:51,870,302A/Guncertain significance
rs77286071320:51,870,356A/Guncertain significance
rs77809611520:51,870,379G/Cuncertain significance
rs100786285220:51,870,508G/Cuncertain significance
rs74531447820:51,870,534G/Cuncertain significance
rs14972413220:51,870,548G/Auncertain significance
rs37010897320:51,870,565A/Guncertain significance
rs145162085820:51,870,659G/Cuncertain significance
rs14756109820:51,870,662C/Tuncertain significance
rs135450868120:51,870,716A/Guncertain significance
rs77361186520:51,870,731G/Auncertain significance
rs14198559920:51,870,755C/Tuncertain significance
rs78082670220:51,870,841G/Auncertain significance
rs14296574320:51,870,845C/Tuncertain significance
rs13884450020:51,870,967G/Auncertain significance
rs199041676620:51,871,010G/Tuncertain significance
rs52885361620:51,871,045G/Auncertain significance
rs77753612420:51,871,072C/Tuncertain significance
rs37251980420:51,871,187C/Tuncertain significance
rs251604857220:51,871,190A/Cuncertain significance
rs91510811020:51,871,216A/Cuncertain significance
rs118734955620:51,871,255G/Cuncertain significance
rs77876999220:51,871,286A/Tlikely benign
rs20075209720:51,871,441G/Auncertain significance
rs36889965520:51,871,448A/Guncertain significance
rs75053062020:51,871,465A/Cuncertain significance
rs14684605420:51,871,636G/Tuncertain significance
rs77713461020:51,871,664C/Tuncertain significance
rs251605084820:51,871,678G/Auncertain significance
rs14568335020:51,871,699C/Tuncertain significance
rs37234755720:51,871,700G/Auncertain significance
rs54339453020:51,871,712C/Tuncertain significance
rs140489808320:51,871,773A/Glikely benign
rs74658750820:51,871,774C/Tuncertain significance
rs13862445120:51,871,781C/Tuncertain significance
rs14932251820:51,871,801A/Guncertain significance
rs14715877620:51,871,858G/Auncertain significance
rs156883793620:51,871,967T/Auncertain significance
rs20053954820:51,872,051A/Guncertain significance
rs75780698420:51,872,057C/Tuncertain significance
rs86700209620:51,872,096C/Tuncertain significance
rs75511928920:51,872,098G/Auncertain significance
rs77157607520:51,872,135T/Cuncertain significance
rs75177730820:51,872,169C/Guncertain significance
rs77901590420:51,872,192C/Tuncertain significance
rs55045747520:51,872,207T/Guncertain significance
rs14700048520:51,872,251G/Auncertain significance
rs77989265520:51,872,260C/Tuncertain significance
rs14358007820:51,872,330C/Tuncertain significance
rs199046165920:51,872,345G/Auncertain significance
rs124335803620:51,872,360A/Guncertain significance
rs77671328120:51,872,398G/Auncertain significance
rs37559532320:51,872,413A/Guncertain significance
rs101351279120:51,872,414C/Guncertain significance
rs141779183320:51,872,450C/Tuncertain significance
rs74738679120:51,872,457G/Tuncertain significance
rs78165897620:51,872,582C/Tuncertain significance
rs75295552420:51,872,782A/Guncertain significance
rs36819258220:51,872,912C/Guncertain significance
rs134745221220:51,872,939C/Guncertain significance
rs124321701220:51,872,998C/Tuncertain significance
rs20035639620:51,873,044C/Tuncertain significance
rs105750921720:52,099,293A/C

Gene information from NCBI Gene. Variant classifications from ClinVar.