UMODL1

uromodulin like 1

Summary

Predicted to enable calcium ion binding activity and peptidase inhibitor activity. Predicted to act upstream of or within several processes, including cellular response to gonadotropin-releasing hormone; regulation of granulosa cell apoptotic process; and regulation of ovarian follicle development. Predicted to be located in cytoplasm; external side of plasma membrane; and extracellular region. Predicted to be active in cell surface and extracellular space. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants153 total

rsidPosition (GRCh37)AllelesClassClinVar
rs37688603521:43,491,439C/T—likely benign
rs90547834521:43,496,240G/A—uncertain significance
rs36848127921:43,496,256G/A—uncertain significance
rs153711621:43,496,292C/T—likely benign
rs20139333421:43,496,305G/A—uncertain significance
rs19964194121:43,496,329G/A—uncertain significance
rs77738003221:43,496,331A/T—uncertain significance
rs19970576521:43,496,339G/A—uncertain significance
rs7595754321:43,501,343G/T——
rs22029921:43,502,762C/G——
rs77580127521:43,504,208G/C—likely benign
rs99158394121:43,504,250C/A—uncertain significance
rs37584349121:43,504,294T/A—likely benign
rs14384339521:43,504,298C/T—likely benign
rs167619641521:43,504,301G/A—uncertain significance
rs76266275921:43,504,323G/C—uncertain significance
rs75164645621:43,504,325G/A—uncertain significance
rs251722454421:43,505,416C/G—uncertain significance
rs251722458921:43,505,425C/T—likely benign
rs20119409321:43,505,434A/G—uncertain significance
rs142096473321:43,505,479T/G—uncertain significance
rs76041400821:43,505,499C/A—uncertain significance
rs37368681421:43,508,423C/A—uncertain significance
rs251723229721:43,508,427G/A—uncertain significance
rs76187516421:43,508,434A/G—likely benign
rs20212297521:43,508,437G/A—likely benign
rs55710672121:43,508,450A/G—uncertain significance
rs77987142421:43,508,451C/G—uncertain significance
rs56564198721:43,508,578G/A—likely benign
rs11710627821:43,508,593T/G—benign
rs18087621821:43,510,398T/C—likely benign
rs76286904921:43,510,463C/T—likely benign
rs53510344421:43,510,480C/T—uncertain significance
rs19202177921:43,510,524C/A—likely benign
rs147591121:43,513,480A/Cregulatory region variant—
rs77867867921:43,519,122C/A—uncertain significance
rs36844467821:43,519,137C/T—likely benign
rs37247286721:43,519,138G/A—likely benign
rs37697103821:43,519,146C/T—uncertain significance
rs77081952521:43,519,195C/T—uncertain significance
rs251725638521:43,519,201C/A—uncertain significance
rs37608553321:43,522,341C/T—uncertain significance
rs91765180921:43,522,350G/T—uncertain significance
rs77021293621:43,522,359C/G—uncertain significance
rs130942886621:43,522,364C/G—uncertain significance
rs37236895621:43,522,385C/A—uncertain significance
rs251726799021:43,524,042T/C—uncertain significance
rs13953605221:43,524,043C/T—benign
rs37566411121:43,524,101G/A—uncertain significance
rs55608526121:43,524,177G/T—uncertain significance
rs1170234721:43,526,454C/Tintron variant—
rs37397320321:43,528,487G/Asynonymous variant—
rs19151514421:43,529,674T/C—uncertain significance
rs122724635621:43,529,756A/G—likely benign
rs20008957521:43,529,762G/A—uncertain significance
rs37291511421:43,529,782C/A—uncertain significance
rs54088633921:43,529,805T/G—uncertain significance
rs104373459921:43,531,016G/A—uncertain significance
rs121127718521:43,531,031A/G—uncertain significance
rs37598335821:43,531,055G/T—uncertain significance
rs147120560721:43,531,115C/T—uncertain significance
rs76350800621:43,531,128C/T—likely benign
rs20036196921:43,531,129G/A—benign
rs54280920721:43,531,142G/A—uncertain significance
rs37524034621:43,531,167G/T—uncertain significance
rs54617509121:43,531,220G/A—uncertain significance
rs74958063921:43,531,257G/T—uncertain significance
rs37074240521:43,531,269G/C—uncertain significance
rs76478075721:43,531,274C/T—uncertain significance
rs88758946621:43,531,298G/A—uncertain significance
rs20073774621:43,531,299G/A—uncertain significance
rs74945627321:43,531,318C/A—uncertain significance
rs77937970821:43,531,328G/A—uncertain significance
rs20175809321:43,531,341A/G—uncertain significance
rs74761407321:43,531,344C/T—uncertain significance
rs251728734621:43,531,361A/C—uncertain significance
rs131554987321:43,531,378C/G—uncertain significance
rs55737710221:43,531,389T/A—uncertain significance
rs75967493621:43,531,454C/T—uncertain significance
rs75279176221:43,531,469C/A—likely benign
rs37536038621:43,531,635T/C—likely benign
rs20164891621:43,531,675C/T—likely benign
rs37036530221:43,531,709C/T—likely benign
rs15052947521:43,533,693C/T—likely benign
rs37494144921:43,533,695T/C—uncertain significance
rs55622407421:43,533,725G/C—uncertain significance
rs20205512321:43,533,797T/C—likely benign
rs37353383321:43,533,892A/C—uncertain significance
rs20215944821:43,535,986C/T—uncertain significance
rs20066466521:43,535,988C/T—likely benign
rs54645704221:43,536,043G/A—uncertain significance
rs75307045321:43,536,058A/C—uncertain significance
rs37409819421:43,536,081C/G—uncertain significance
rs37690181321:43,539,225G/A—uncertain significance
rs14028046521:43,539,262C/T—likely benign
rs54315251621:43,539,264C/T—uncertain significance
rs20062657221:43,539,311G/C—uncertain significance
rs37649947121:43,539,337C/T—likely benign
rs75802839421:43,539,360T/C—uncertain significance
rs75493548321:43,541,230G/A—uncertain significance

Showing 100 of 153 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.