ERG

ETS transcription factor ERG

Summary

This gene encodes a member of the erythroblast transformation-specific (ETS) family of transcriptions factors. All members of this family are key regulators of embryonic development, cell proliferation, differentiation, angiogenesis, inflammation, and apoptosis. The protein encoded by this gene is mainly expressed in the nucleus. It contains an ETS DNA-binding domain and a PNT (pointed) domain which is implicated in the self-association of chimeric oncoproteins. This protein is required for platelet adhesion to the subendothelium, inducing vascular cell remodeling. It also regulates hematopoesis, and the differentiation and maturation of megakaryocytic cells. This gene is involved in chromosomal translocations, resulting in different fusion gene products, such as TMPSSR2-ERG and NDRG1-ERG in prostate cancer, EWS-ERG in Ewing's sarcoma and FUS-ERG in acute myeloid leukemia. More than two dozens of transcript variants generated from combinatorial usage of three alternative promoters and multiple alternative splicing events have been reported, but the full-length nature of many of these variants has not been determined. [provided by RefSeq, Apr 2014]

Known Variants36 total

rsidPosition (GRCh37)AllelesClassClinVar
rs53010462521:39,755,360T/Cuncertain significance
rs53137781121:39,755,459G/Auncertain significance
rs20099507321:39,755,468G/Auncertain significance
rs214641234121:39,755,663C/Tuncertain significance
rs251699862921:39,755,677T/Cuncertain significance
rs214641241521:39,755,678C/Tuncertain significance
rs55741987721:39,764,304A/Tuncertain significance
rs139577276621:39,764,352G/Auncertain significance
rs198844440221:39,772,564C/Auncertain significance
rs14992886521:39,774,495C/Tuncertain significance
rs142245644621:39,775,539G/Cuncertain significance
rs18462964521:39,785,989G/Aregulatory region variant
rs98955421:39,786,927G/Aintron variant
rs77458019521:39,795,357G/Alikely benign
rs77224814921:39,795,361G/Tuncertain significance
rs76065536421:39,795,373G/Cuncertain significance
rs76857756921:39,795,460A/Guncertain significance
rs13917163421:39,795,466C/Tuncertain significance
rs283640521:39,816,771G/T
rs76995725221:39,817,445C/Tuncertain significance
rs251675531921:39,817,453G/Auncertain significance
rs283641121:39,819,830C/Tregulatory region variant
rs378790121:39,840,825G/Aintron variant
rs3482596921:39,846,142G/Aregulatory region variant
rs1305210721:39,848,961A/Gregulatory region variant
rs727521221:39,852,551A/Tintron variant
rs5803028821:39,854,478C/A
rs7427653121:39,856,202T/Aintron variant
rs101376621:39,856,415G/Aregulatory region variant
rs1305241821:39,857,628A/T
rs283643821:39,864,727A/T
rs283644121:39,870,310G/Aregulatory region variant
rs54757838021:39,874,468T/Cuncertain significance
rs1170122721:39,906,783C/Tintron variant
rs20130278821:39,947,608G/Auncertain significance
rs221259621:39,968,534A/Cintron variant

Gene information from NCBI Gene. Variant classifications from ClinVar.