OGDHL

oxoglutarate dehydrogenase L

Summary

The protein encoded by this gene is similar to oxoglutarate dehydrogenase (OGDH) of the OGDH complex, which degrades glucose and glutamate. This gene encodes several isoforms, including some that appear to localize to mitochondria. The encoded protein down-regulates the AKT signaling cascade and can suppress the growth of cervical cancer cells. [provided by RefSeq, Dec 2016]

Known Variants103 total

rsidPosition (GRCh37)AllelesClassClinVar
rs375075510:50,943,248G/A3 prime UTR variant—
rs13877020710:50,943,323A/C—uncertain significance
rs14314704310:50,943,339C/G—uncertain significance
rs11301430610:50,943,376C/T—benign
rs74829732210:50,944,084C/T—uncertain significance
rs7537264610:50,944,160C/T—likely benign
rs76807527010:50,944,168G/A—uncertain significance
rs19967565310:50,944,415C/T—likely benign
rs15130496210:50,944,490G/A—likely benign
rs20046364210:50,944,517G/A—likely benign
rs14028143910:50,944,528C/A—likely benign
rs1235725510:50,944,529G/A—benign
rs20127650210:50,944,530G/A—uncertain significance
rs76885360510:50,944,551C/T—uncertain significance
rs213294466110:50,945,868G/C—uncertain significance
rs253895223810:50,945,886T/C—uncertain significance
rs4128197110:50,945,890T/G—likely benign
rs77388830810:50,946,295G/Amissense variantpathogenic
rs20218523610:50,946,307C/T—uncertain significance
rs253896245810:50,947,726G/A—uncertain significance
rs75255293210:50,947,730G/T—uncertain significance
rs75677451910:50,947,753C/T—uncertain significance
rs77847489810:50,947,754G/A—uncertain significance
rs13813851010:50,947,807G/A—uncertain significance
rs14310528810:50,947,825A/G—likely benign
rs14749377610:50,947,844C/T—uncertain significance
rs229323910:50,947,852T/A—affects
rs7279576510:50,948,489G/Aintron variant—
rs184158377110:50,948,755C/T—likely pathogenic
rs119306042310:50,948,846G/A—uncertain significance
rs146294830110:50,948,878C/T—pathogenic
rs14792409610:50,950,891C/T—likely benign
rs95693740810:50,950,902C/T—uncertain significance
rs3561362810:50,950,903G/A—benign
rs124582883110:50,950,971C/T—uncertain significance
rs1110122410:50,950,976G/A—benign
rs37397491910:50,950,979C/T—uncertain significance
rs77368349410:50,950,980G/A—uncertain significance
rs14133515110:50,950,997G/A—benign
rs13973161210:50,951,001G/A—uncertain significance
rs3487719510:50,951,018G/C—likely benign
rs253898901410:50,951,026T/C—likely pathogenic
rs4128198110:50,952,033A/G—likely benign
rs118499868710:50,952,059C/G—uncertain significance
rs14389807910:50,952,084C/T—uncertain significance
rs13986743010:50,952,088C/A—conflicting classifications of pathogenicity
rs20148667010:50,952,091T/C—uncertain significance
rs138749020510:50,952,168C/G—uncertain significance
rs122672911810:50,952,708A/G—uncertain significance
rs253900132610:50,953,401G/T—uncertain significance
rs137702380610:50,953,460T/C—uncertain significance
rs55147815610:50,953,506C/T—uncertain significance
rs791011410:50,953,830A/G—benign
rs213302873510:50,953,856A/G—pathogenic
rs77454777610:50,953,977G/A—uncertain significance
rs14545814810:50,954,027C/T—likely benign
rs75952947810:50,954,827T/C—uncertain significance
rs75563435110:50,954,833G/A—uncertain significance
rs7597453010:50,954,850G/A—benign
rs14612953410:50,954,868A/G—benign
rs20097638810:50,954,898G/A—likely benign
rs75266309110:50,955,125C/G—uncertain significance
rs3436988710:50,955,152G/A—benign
rs184225104610:50,955,170C/T—uncertain significance
rs3590295710:50,955,185T/G—uncertain significance
rs130322250810:50,955,226C/A—uncertain significance
rs125817910:50,957,514G/Aintron variant—
rs253902309010:50,957,825C/G—uncertain significance
rs75669869210:50,957,849C/T—uncertain significance
rs92497541310:50,958,886T/C—likely pathogenic
rs15023196710:50,958,895T/Amissense variantlikely benign
rs77117482510:50,958,925C/T—uncertain significance
rs119753068610:50,958,958G/A—uncertain significance
rs75035574610:50,958,973A/G—uncertain significance
rs127772632510:50,959,003A/G—uncertain significance
rs125818210:50,959,682C/Gintron variant—
rs77281990510:50,959,892G/A—uncertain significance
rs13988817710:50,959,950C/G—uncertain significance
rs15073413110:50,960,190G/A—uncertain significance
rs76076416310:50,960,202G/A—uncertain significance
rs125818410:50,960,209G/A—benign
rs119870393110:50,960,225C/T—uncertain significance
rs14714353610:50,960,231A/G—uncertain significance
rs184265107110:50,960,240G/A—uncertain significance
rs7688907710:50,960,281A/C—likely benign
rs253903741410:50,960,290G/C—uncertain significance
rs37435453010:50,960,717G/A—uncertain significance
rs14506318010:50,960,718C/Asynonymous variant—
rs127210876410:50,960,747T/G—uncertain significance
rs77307044110:50,960,783G/A—uncertain significance
rs14262280310:50,964,883G/T—conflicting classifications of pathogenicity
rs77844770010:50,964,947C/T—uncertain significance
rs14562127610:50,966,447C/T—likely benign
rs77080705010:50,966,472T/C—uncertain significance
rs14518348910:50,966,510G/A—likely benign
rs253906327510:50,966,512T/C—uncertain significance
rs253906329410:50,966,515T/C—uncertain significance
rs76229044910:50,966,520A/G—uncertain significance
rs13894951410:50,966,528C/T—likely benign
rs76291748010:50,966,529G/A—uncertain significance

Showing 100 of 103 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.