CD164

CD164 molecule

Summary

This gene encodes a transmembrane sialomucin and cell adhesion molecule that regulates the proliferation, adhesion and migration of hematopoietic progenitor cells. The encoded protein also interacts with the C-X-C chemokine receptor type 4 and may regulate muscle development. Elevated expression of this gene has been observed in human patients with Sezary syndrome, a type of blood cancer, and a mutation in this gene may be associated with impaired hearing. [provided by RefSeq, Oct 2016]

Known Variants93 total

rsidPosition (GRCh37)AllelesClassClinVar
rs9740346:109,689,431A/G—benign
rs1471435776:109,689,521T/A—likely benign
rs94870746:109,689,681T/C—benign
rs5546063036:109,689,734G/C—likely benign
rs94870756:109,689,902C/T—benign
rs112516:109,689,907G/T—benign
rs7576455366:109,690,057C/T—likely benign
rs624361046:109,690,073C/T—likely benign
rs8766614026:109,690,074G/Astop gainedno classifications from unflagged records
rs11660706826:109,690,077C/T—uncertain significance
rs7804245426:109,690,085T/C—uncertain significance
rs7465897026:109,690,091A/T—uncertain significance
rs3755535906:109,690,099A/C—likely benign
rs1473934586:109,690,100A/G—uncertain significance
rs7730999236:109,690,107A/G—uncertain significance
rs7520475976:109,690,198A/C—likely benign
rs3685144106:109,690,232G/C—benign
rs1170304546:109,690,517A/G—likely benign
rs22756496:109,691,328T/C—benign
rs3718195916:109,691,598A/G—likely benign
rs5622389366:109,691,621A/C—likely benign
rs1452699756:109,691,627T/C—likely benign
rs7482763446:109,691,632T/G—uncertain significance
rs21151440526:109,691,637G/T—uncertain significance
rs94809416:109,691,639T/C—benign
rs1487003196:109,691,641T/C—uncertain significance
rs7666024256:109,691,644A/G—uncertain significance
rs7679745186:109,691,663G/A—benign
rs3695265326:109,691,688T/G—likely benign
rs1150997236:109,691,766T/C—benign
rs38189336:109,691,944G/A—benign
rs94870766:109,692,727T/Cintron variant—
rs117536456:109,695,054T/Cregulatory region variant—
rs341316796:109,697,051C/A—benign
rs1456662406:109,697,083T/C—likely benign
rs7716016496:109,697,285T/C—uncertain significance
rs3739060876:109,697,308C/T—likely benign
rs12658384416:109,697,319T/C—uncertain significance
rs1176683716:109,697,599A/C—benign
rs1149954686:109,699,045C/G—likely benign
rs3775051316:109,699,092T/G—likely benign
rs1420436306:109,699,103C/T—uncertain significance
rs1998876086:109,699,104G/A—conflicting classifications of pathogenicity
rs7526392596:109,699,131T/A—uncertain significance
rs14511156116:109,699,152G/A—likely benign
rs5560255726:109,699,158T/C—likely benign
rs10488612196:109,699,159G/A—uncertain significance
rs3762610796:109,699,171T/C—uncertain significance
rs7577645386:109,699,182G/A—likely benign
rs15622420016:109,699,185G/A—likely benign
rs14076206:109,699,359C/T—benign
rs354528366:109,699,446A/T—benign
rs775042656:109,700,632C/A—benign
rs1421902276:109,700,762G/C—benign
rs24824550206:109,700,764A/C—likely benign
rs24824550566:109,700,770A/C—likely benign
rs2011686216:109,700,808G/A—uncertain significance
rs7629774396:109,700,820C/T—likely benign
rs12702802496:109,700,832C/T—likely benign
rs1453573326:109,700,847T/C—likely benign
rs1913868416:109,700,851G/C—likely benign
rs3772622946:109,700,856T/C—uncertain significance
rs1392183226:109,700,873G/A—likely benign
rs5516979416:109,700,877G/A—likely benign
rs7752231406:109,700,881G/C—likely benign
rs22756516:109,701,056T/G—benign
rs14863494836:109,702,718G/C—likely benign
rs5481295246:109,702,767T/A—benign
rs737627156:109,702,776G/A—benign
rs5327502746:109,703,170C/G—benign
rs119631336:109,703,241G/C—benign
rs774989536:109,703,307C/T—benign
rs43130336:109,703,327G/A—likely benign
rs18856916:109,703,391C/T—benign
rs11924355986:109,703,414C/G—likely benign
rs24824739426:109,703,419T/A—likely benign
rs1139022286:109,703,451G/A—likely benign
rs7479901846:109,703,459G/A—likely benign
rs21151770236:109,703,469G/A—uncertain significance
rs24824746976:109,703,470G/C—uncertain significance
rs7507808676:109,703,494G/A—uncertain significance
rs1389256986:109,703,524C/A—uncertain significance
rs7756307956:109,703,545T/C—likely benign
rs7619935486:109,703,557G/A—uncertain significance
rs3731950636:109,703,567G/A—likely benign
rs3761418426:109,703,584T/C—likely benign
rs14909043516:109,703,593C/T—uncertain significance
rs1908427826:109,703,622G/C—benign
rs22756526:109,703,683G/C—benign
rs13228166:109,703,727C/A—benign
rs1152250986:109,703,868A/T—likely benign
rs13228156:109,704,062A/G—benign
rs1157052326:109,704,091G/A—benign

Gene information from NCBI Gene. Variant classifications from ClinVar.