CDHR3

cadherin related family member 3

Summary

Predicted to enable beta-catenin binding activity and cadherin binding activity. Predicted to be involved in several processes, including calcium-dependent cell-cell adhesion via plasma membrane cell adhesion molecules; cell-cell adhesion mediated by cadherin; and cell-cell junction organization. Located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants71 total

rsidPosition (GRCh37)AllelesClassClinVar
rs27277537:105,608,411A/Tintron variant—
rs27277577:105,612,736A/C——
rs12039320907:105,615,290G/C—uncertain significance
rs2015631717:105,615,326C/T—likely benign
rs7583303877:105,615,370A/C—uncertain significance
rs1937967:105,620,291G/Aintron variant—
rs2008927417:105,621,462A/G—uncertain significance
rs24853536327:105,621,495G/T—uncertain significance
rs7755016897:105,624,646C/A—uncertain significance
rs14718447797:105,635,216C/A—uncertain significance
rs2014304987:105,635,285A/G—uncertain significance
rs2000194717:105,636,709G/A—uncertain significance
rs8873261537:105,636,716T/G—uncertain significance
rs14897885687:105,636,726T/C—likely benign
rs5352385007:105,636,778G/A—uncertain significance
rs2015950887:105,636,790C/T—uncertain significance
rs2006232697:105,636,791G/A—likely benign
rs10242060157:105,641,952C/A—uncertain significance
rs24854185887:105,642,030T/C—uncertain significance
rs24854185937:105,642,032A/G—uncertain significance
rs7493416877:105,645,063C/A—uncertain significance
rs3736914517:105,645,064G/T—uncertain significance
rs77835277:105,645,092C/T—benign
rs2010556227:105,645,122G/T—uncertain significance
rs24854476407:105,653,316C/T—uncertain significance
rs2022049667:105,653,317C/T—uncertain significance
rs2001027937:105,653,388C/T—uncertain significance
rs24854479687:105,653,416C/G—uncertain significance
rs796866957:105,653,450G/A—benign
rs3689260027:105,655,577C/T—likely benign
rs13742349417:105,655,617G/A—uncertain significance
rs2020057677:105,656,377C/T—likely benign
rs1867259397:105,656,378G/A—likely benign
rs1932790797:105,656,384G/A—likely benign
rs24854570307:105,656,415T/G—uncertain significance
rs7588180937:105,656,436C/T—uncertain significance
rs3772715697:105,656,442A/C—uncertain significance
rs7492349187:105,656,463G/T—uncertain significance
rs1434959087:105,656,471G/A—likely benign
rs13020950457:105,658,301G/T—uncertain significance
rs1824559357:105,658,316G/A—likely benign
rs760677977:105,658,381C/T—conflicting classifications of pathogenicity
rs14570802417:105,658,426C/T—uncertain significance
rs69673307:105,658,451G/Amissense variant—
rs1177976547:105,658,521A/G—likely benign
rs13474565597:105,660,940G/A—uncertain significance
rs1449058887:105,660,972C/T—likely benign
rs3686243247:105,660,978T/A—uncertain significance
rs15633008077:105,662,653A/G—uncertain significance
rs2006399307:105,662,697C/T—uncertain significance
rs3691440107:105,662,698G/A—uncertain significance
rs2012584357:105,662,766G/T—uncertain significance
rs7684896717:105,662,884C/T—uncertain significance
rs14020656627:105,664,864A/G—uncertain significance
rs3761512537:105,664,873C/G—uncertain significance
rs7779153597:105,664,893G/A—uncertain significance
rs12691818877:105,664,912T/C—uncertain significance
rs7737734597:105,664,932G/A—uncertain significance
rs2019692687:105,664,935T/C—uncertain significance
rs115058867:105,664,944G/A—likely benign
rs2005855717:105,665,002A/C—uncertain significance
rs3733628997:105,667,145T/G—likely benign
rs3685557677:105,671,248A/G—uncertain significance
rs102703087:105,671,267T/Csynonymous variant—
rs7555446677:105,671,269G/C—uncertain significance
rs24855046587:105,672,872C/T—uncertain significance
rs1408187207:105,672,877G/T—likely benign
rs3710078707:105,672,944C/T—uncertain significance
rs7791620257:105,672,949C/T—likely benign
rs3767279417:105,672,955G/C—uncertain significance
rs5570324537:105,673,033G/A—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.