ADH1C

alcohol dehydrogenase 1C (class I), gamma polypeptide

Summary

This gene encodes class I alcohol dehydrogenase, gamma subunit, which is a member of the alcohol dehydrogenase family. Members of this enzyme family metabolize a wide variety of substrates, including ethanol, retinol, other aliphatic alcohols, hydroxysteroids, and lipid peroxidation products. Class I alcohol dehydrogenase, consisting of several homo- and heterodimers of alpha, beta, and gamma subunits, exhibits high activity for ethanol oxidation to acetaldehyde, thus playing a major role in ethanol catabolism. Three genes encoding alpha, beta and gamma subunits are tandemly organized in a genomic segment as a gene cluster. An association between ADH1C polymorphism and alcohol dependence has not been established. [provided by RefSeq, Sep 2019]

Known Variants39 total

rsidPosition (GRCh37)AllelesClassClinVar
rs7744843944:100,257,924G/A—likely benign
rs16127354:100,258,007T/Cintron variant—
rs16149724:100,258,155C/G——
rs38464494:100,259,126T/Cintron variant—
rs16934564:100,259,351G/T——
rs623072954:100,260,545C/Aintron variant—
rs5612228714:100,260,679C/T——
rs13393406874:100,260,771T/C—uncertain significance
rs357195134:100,260,783G/T—benign
rs6984:100,260,789A/Gmissense variantprotective
rs22987554:100,261,038C/A——
rs7691215424:100,261,758C/T—uncertain significance
rs7514353734:100,261,813C/G—uncertain significance
rs2002533594:100,261,822T/A—uncertain significance
rs14044102244:100,261,857A/C—uncertain significance
rs17899034:100,262,041C/A——
rs1419739044:100,262,242C/Tintron variant—
rs64134464:100,263,945A/T—likely benign
rs5536512244:100,263,946T/A—likely benign
rs16934824:100,263,965C/Tmissense variantprotective
rs64134444:100,264,102G/A—benign
rs7481914994:100,264,157A/G—likely benign
rs2834114:100,265,957C/T——
rs10011089354:100,266,030T/C—uncertain significance
rs557179074:100,266,064G/A—likely benign
rs5419248844:100,266,095G/A—uncertain significance
rs25301918064:100,266,150T/A—uncertain significance
rs793720274:100,266,157G/A—likely benign
rs357256084:100,266,163G/A—likely benign
rs11921953224:100,266,215A/G—uncertain significance
rs7782989934:100,266,227G/C—uncertain significance
rs2834134:100,268,190A/Cstop lostrisk factor
rs25301965594:100,268,205T/C—uncertain significance
rs7701180584:100,268,231A/G—likely benign
rs25301967784:100,268,267T/A—uncertain significance
rs353859024:100,268,279C/T—benign
rs25301982934:100,268,972T/G—uncertain significance
rs131471894:100,270,256T/A——
rs17899244:100,274,286C/Tupstream gene variant—

Gene information from NCBI Gene. Variant classifications from ClinVar.