HECTD4

HECT domain E3 ubiquitin protein ligase 4

Summary

Predicted to enable ubiquitin-protein transferase activity. Involved in glucose homeostasis and glucose metabolic process. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants211 total

rsidPosition (GRCh37)AllelesClassClinVar
rs18388278412:112,600,883C/T—likely benign
rs203079067312:112,601,354A/C—uncertain significance
rs98868490912:112,601,368T/C—uncertain significance
rs203079427612:112,601,414T/C—uncertain significance
rs18163493812:112,601,455C/T—uncertain significance
rs144804484212:112,601,464G/A—uncertain significance
rs249972506312:112,601,500A/C—uncertain significance
rs6174883912:112,601,517C/T—likely benign
rs96706554612:112,601,525T/C—uncertain significance
rs116016333812:112,601,920G/C—uncertain significance
rs20211942512:112,601,928C/T—uncertain significance
rs20026840412:112,602,018G/A—uncertain significance
rs88975322112:112,605,122C/G—uncertain significance
rs36771375112:112,605,138C/T—uncertain significance
rs18966751312:112,605,167T/C—likely benign
rs37193587512:112,605,195C/T—uncertain significance
rs13866956612:112,605,196G/A—benign
rs14169928012:112,605,247G/A—benign
rs249973619412:112,605,305C/G—uncertain significance
rs37691917612:112,605,311G/A—uncertain significance
rs75461175812:112,605,661G/A—uncertain significance
rs77935573712:112,605,673C/T—uncertain significance
rs76897275612:112,605,691A/G—uncertain significance
rs55796885012:112,605,720G/A—likely benign
rs37055506012:112,608,146T/C—uncertain significance
rs18688497112:112,608,227C/T—likely benign
rs249974466812:112,608,245A/G—uncertain significance
rs97190961412:112,608,990G/T—uncertain significance
rs797018112:112,609,998C/Tintron variant—
rs6199931112:112,610,487C/T—uncertain significance
rs78029151912:112,610,490C/T—uncertain significance
rs36908329112:112,610,512G/A—likely benign
rs78144045512:112,610,567C/T—uncertain significance
rs213700951812:112,610,616T/C—uncertain significance
rs77551460712:112,613,586C/T—uncertain significance
rs75448394912:112,613,609C/T—uncertain significance
rs249975877812:112,613,655C/T—uncertain significance
rs20136318712:112,616,770C/T—benign
rs249976591012:112,616,792G/A—uncertain significance
rs74721632412:112,617,007T/C—uncertain significance
rs37438304412:112,617,097C/T—uncertain significance
rs101128015512:112,617,103T/C—uncertain significance
rs75593741312:112,617,174T/C—uncertain significance
rs77173869512:112,620,889T/C—uncertain significance
rs203173945712:112,620,973A/G—uncertain significance
rs132312173312:112,622,026C/T—likely benign
rs20155334712:112,622,044G/C—likely benign
rs37354080612:112,622,184G/A—likely benign
rs93070150512:112,622,204C/T—likely benign
rs78110332512:112,622,238G/A—uncertain significance
rs36969255312:112,622,244A/G—uncertain significance
rs55988619512:112,622,256C/A—uncertain significance
rs78168894912:112,622,321G/C—uncertain significance
rs249977641412:112,622,439G/C—uncertain significance
rs249977664712:112,622,551G/A—pathogenic
rs249977691212:112,622,670A/G—uncertain significance
rs155524831112:112,622,785G/A—pathogenic
rs249977734312:112,622,834C/A—uncertain significance
rs86778251212:112,622,938T/C—uncertain significance
rs127924365312:112,622,998T/A—uncertain significance
rs77446568412:112,623,015G/A—uncertain significance
rs140992348612:112,623,039G/A—uncertain significance
rs132770084012:112,623,051C/G—uncertain significance
rs131896756612:112,623,054G/A—uncertain significance
rs144178879612:112,623,057C/T—uncertain significance
rs75731845312:112,623,067C/T—likely benign
rs36910036712:112,623,070C/T—likely benign
rs213702896212:112,623,086C/G—uncertain significance
rs116221923112:112,623,123T/G—uncertain significance
rs92265739112:112,623,180A/G—uncertain significance
rs76180829912:112,623,200C/G—uncertain significance
rs14450427112:112,627,350G/Aintron variant—
rs37029131412:112,628,617C/T—uncertain significance
rs20053806512:112,628,647C/T—uncertain significance
rs55534641212:112,629,667G/C——
rs37130427412:112,630,463G/A—uncertain significance
rs249979682012:112,630,538C/A—uncertain significance
rs135649302412:112,630,549G/A—uncertain significance
rs77256703612:112,630,872G/A—uncertain significance
rs249979792412:112,630,877C/G—uncertain significance
rs54541376312:112,630,959T/C—uncertain significance
rs37462065312:112,631,298G/A—uncertain significance
rs76740981012:112,631,323C/A—uncertain significance
rs37763258412:112,631,327G/C—uncertain significance
rs37076336312:112,631,404C/T—uncertain significance
rs203215291112:112,631,459G/C—uncertain significance
rs54708202912:112,632,776G/A—uncertain significance
rs75907569212:112,632,859C/T—uncertain significance
rs99785229512:112,632,860G/A—uncertain significance
rs77959096512:112,638,584C/T—uncertain significance
rs249982235512:112,641,540T/A—uncertain significance
rs207435612:112,645,401G/Aintron variant—
rs249983215812:112,645,713G/A—uncertain significance
rs129969735212:112,646,299T/C—uncertain significance
rs75728512812:112,646,399C/T—uncertain significance
rs249983810212:112,647,860C/T—uncertain significance
rs37666605912:112,647,888T/C—uncertain significance
rs77399614512:112,647,989T/C—uncertain significance
rs53289964612:112,647,999C/T—uncertain significance
rs90336298912:112,648,010G/A—uncertain significance

Showing 100 of 211 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.