NCOR2

nuclear receptor corepressor 2

Summary

This gene encodes a nuclear receptor co-repressor that mediates transcriptional silencing of certain target genes. The encoded protein is a member of a family of thyroid hormone- and retinoic acid receptor-associated co-repressors. This protein acts as part of a multisubunit complex which includes histone deacetylases to modify chromatin structure that prevents basal transcriptional activity of target genes. Aberrant expression of this gene is associated with certain cancers. Alternate splicing results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Apr 2011]

Known Variants326 total

rsidPosition (GRCh37)AllelesClassClinVar
rs854612:124,809,027G/Aregulatory region variant—
rs254737803312:124,809,956T/A—uncertain significance
rs89771043412:124,809,959C/A—uncertain significance
rs254737805712:124,809,965G/C—uncertain significance
rs203454228012:124,809,967G/C—uncertain significance
rs159305132012:124,809,973T/G—uncertain significance
rs203454276512:124,809,976T/A—uncertain significance
rs100725561512:124,809,977G/T—uncertain significance
rs203454344012:124,809,992G/A—uncertain significance
rs98582841212:124,810,010A/G—uncertain significance
rs140229508712:124,810,016G/A—uncertain significance
rs7710780112:124,810,028C/T—benign
rs148800157812:124,810,045G/A—uncertain significance
rs74531203512:124,810,046C/T—uncertain significance
rs74920830812:124,810,060G/A—uncertain significance
rs77212215512:124,810,083C/T—likely benign
rs20031211412:124,810,093C/T—uncertain significance
rs18901370412:124,810,134G/A—likely benign
rs1105758312:124,810,329G/Aintron variant—
rs19964635812:124,810,741G/A—likely benign
rs75191922812:124,810,766C/T—uncertain significance
rs76035821312:124,810,767G/A—uncertain significance
rs18735010512:124,810,804C/T—benign
rs6174431112:124,810,837C/A—benign
rs75830492412:124,810,868G/A—uncertain significance
rs19976259012:124,810,911C/T—uncertain significance
rs74936159412:124,810,912G/A—likely benign
rs20151359912:124,811,994C/T—uncertain significance
rs19961666412:124,812,062G/A—uncertain significance
rs77092048912:124,812,069A/T—uncertain significance
rs254738523312:124,812,134G/C—uncertain significance
rs37006438912:124,812,167T/C—likely benign
rs254740217512:124,817,005C/T—uncertain significance
rs18815439312:124,817,711C/T—likely benign
rs20190436812:124,817,719C/T—likely benign
rs19959368112:124,817,732G/A—likely benign
rs7536267712:124,817,756C/T—likely benign
rs75025294812:124,817,767C/A—uncertain significance
rs147284012:124,817,806T/G—benign
rs36961288012:124,818,975G/C—likely benign
rs18107234112:124,818,984G/A—benign
rs37704512612:124,818,994G/T—uncertain significance
rs20185308612:124,819,002G/C—likely benign
rs75803875512:124,819,027G/A—uncertain significance
rs77442168512:124,819,054C/T—uncertain significance
rs76189215712:124,819,055G/A—uncertain significance
rs74904166412:124,819,116G/A—likely benign
rs37675789112:124,819,673G/A—likely benign
rs89308639612:124,819,746G/T—uncertain significance
rs3598049312:124,819,747C/T—benign
rs19989927612:124,819,748G/A—uncertain significance
rs129108165112:124,819,772G/A—uncertain significance
rs14702067712:124,819,800C/T—uncertain significance
rs110631712:124,820,013A/G—benign
rs20176655712:124,820,043C/T—uncertain significance
rs125825167812:124,820,059G/C—uncertain significance
rs77503158912:124,820,104C/T—uncertain significance
rs11651177712:124,820,138G/A—benign
rs76651473412:124,820,157C/G—uncertain significance
rs125025713212:124,821,367G/A—uncertain significance
rs76235279012:124,821,373G/A—likely benign
rs37164118112:124,821,384C/T—likely benign
rs75630417212:124,821,391G/A—uncertain significance
rs76869719312:124,821,397G/A—uncertain significance
rs11528713812:124,821,403G/A—benign
rs223094412:124,821,413A/G—benign
rs222727712:124,821,416C/T—benign
rs36784166912:124,821,430G/T—uncertain significance
rs37128519712:124,821,436C/T—uncertain significance
rs36851856812:124,821,440C/T—uncertain significance
rs37251219512:124,821,449C/T—uncertain significance
rs223094312:124,821,483C/A—benign
rs75363416712:124,821,486C/T—likely benign
rs159310784112:124,821,505G/T—likely pathogenic
rs37683335312:124,821,522G/A—likely benign
rs75765062712:124,821,568C/T—uncertain significance
rs93268095912:124,821,574C/T—uncertain significance
rs77651771912:124,821,593G/A—uncertain significance
rs19972916312:124,821,618G/A—benign
rs138630196112:124,821,655C/T—uncertain significance
rs19231935112:124,821,656C/T—likely benign
rs139242426612:124,821,662G/C—uncertain significance
rs6175135412:124,821,666G/A—benign
rs222984212:124,821,696C/T—benign
rs37584672412:124,821,704C/T—uncertain significance
rs374151212:124,821,705G/A—benign
rs37684494812:124,824,583C/T—uncertain significance
rs36786639312:124,824,585G/T—uncertain significance
rs20210637312:124,824,613G/A—uncertain significance
rs36906228312:124,824,641A/T—uncertain significance
rs76439689912:124,824,690G/C—uncertain significance
rs20048867512:124,824,694C/A—uncertain significance
rs57774590212:124,824,703T/C—uncertain significance
rs254743328212:124,824,873T/C—uncertain significance
rs37522911812:124,824,906G/A—uncertain significance
rs75400804412:124,824,912G/A—uncertain significance
rs74768523712:124,824,949C/T—likely benign
rs77477566612:124,825,174C/T—uncertain significance
rs1242260712:124,825,175G/A—uncertain significance
rs118582784012:124,825,229T/A—uncertain significance

Showing 100 of 326 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.

NCOR2 — nuclear receptor corepressor 2