DCDC1

doublecortin domain containing 1

Summary

This gene encodes a member of the doublecortin family. The protein encoded by this gene is a hydrophilic, intracellular protein. It contains a single doublecortin domain and is unable to bind microtubules and to regulate microtubule polymerization. This gene is mainly expressed in adult testis. It does not have a mouse homolog. [provided by RefSeq, Sep 2010]

Known Variants82 total

rsidPosition (GRCh37)AllelesClassClinVar
rs5571924111:30,902,837A/G—benign
rs75163704311:30,915,875G/T—uncertain significance
rs37744573811:30,921,117G/A—uncertain significance
rs7560620511:30,921,152C/G—benign
rs11739619711:30,921,166T/C—benign
rs3411066111:30,925,058T/C—benign
rs194485396211:30,925,092C/T—uncertain significance
rs36905335211:30,925,160G/A—uncertain significance
rs6174765611:30,926,525C/T—benign
rs77762430311:30,926,701G/A—uncertain significance
rs37671727111:30,928,101T/C—likely benign
rs249481620911:30,928,202C/T—uncertain significance
rs13857054911:30,938,459T/C—uncertain significance
rs14342854111:30,942,438G/A—benign
rs14474789111:30,946,907A/T—uncertain significance
rs53538912211:30,946,920C/T—uncertain significance
rs16387911:30,951,674C/Tintron variant—
rs15099751411:30,953,328G/A—likely benign
rs14667600211:30,953,418A/G—uncertain significance
rs78066972711:30,974,054T/C—likely benign
rs15863311:30,974,115C/A—benign
rs14347398011:30,997,907C/Tintron variant—
rs7898677511:31,055,942C/Tintron variant—
rs51420711:31,079,119G/C——
rs70468611:31,084,514C/Tintron variant—
rs28908011:31,086,115G/T—benign
rs18904196911:31,086,691G/C—benign
rs53452062611:31,099,404G/A—benign
rs15060368011:31,099,456A/C—benign
rs61974511:31,106,725A/C——
rs91904511:31,111,810T/Cintron variant—
rs15005672411:31,112,984A/G—likely benign
rs37111086411:31,115,663T/C—likely benign
rs36773094211:31,123,714A/G—likely benign
rs18355589911:31,123,752T/C—likely benign
rs20807911:31,128,152C/Gintron variant—
rs8029956811:31,128,438T/C—benign
rs11603835911:31,128,479T/C—likely benign
rs7524943011:31,149,044G/A—benign
rs36855800611:31,149,080T/C—likely benign
rs20809111:31,190,099G/Cintron variant—
rs15814611:31,210,433G/T——
rs1692191411:31,210,771G/C——
rs255405311:31,233,857A/Cintron variant—
rs14120931311:31,284,619T/C—benign
rs76947158311:31,287,078T/C—uncertain significance
rs77241356611:31,287,093A/T—uncertain significance
rs14939358211:31,287,107G/T—uncertain significance
rs94793846811:31,287,156G/A—likely benign
rs20197049011:31,312,181A/G—benign
rs20103984111:31,312,205T/C—uncertain significance
rs194716590911:31,312,274A/G—uncertain significance
rs76488473511:31,312,303A/G—uncertain significance
rs37712107211:31,312,310G/A—uncertain significance
rs78143782111:31,312,327C/T—likely benign
rs253966950111:31,312,339T/A—uncertain significance
rs37168872611:31,312,343T/C—uncertain significance
rs261679211:31,324,298T/A——
rs19981158011:31,327,153C/A—likely benign
rs127234981511:31,327,171T/G—uncertain significance
rs77386745811:31,327,199C/T—likely benign
rs14075860611:31,327,200G/A—uncertain significance
rs14350670311:31,327,244G/C—benign
rs120775009711:31,327,268G/C—uncertain significance
rs75063600911:31,327,300G/A—likely benign
rs261681511:31,327,316C/T—benign
rs18271563511:31,327,342G/A—benign
rs276159211:31,327,766G/A—benign
rs76315892611:31,327,808C/A—uncertain significance
rs1692206611:31,327,836A/C—benign
rs253979189811:31,327,894T/C—uncertain significance
rs74760110411:31,327,896C/A—likely benign
rs76188471911:31,329,335T/A—uncertain significance
rs253980431411:31,329,358C/T—uncertain significance
rs276159111:31,329,373C/T—benign
rs14644055711:31,329,415T/C—uncertain significance
rs14078394411:31,329,438T/C—uncertain significance
rs1012875311:31,335,424C/Aintron variant—
rs6187988411:31,349,483G/Cintron variant—
rs77802260011:31,349,661T/C—likely benign
rs1103135711:31,349,808T/C—benign
rs648450011:31,355,524A/G——

Gene information from NCBI Gene. Variant classifications from ClinVar.