LGALS8

galectin 8

Summary

This gene encodes a member of the galectin family. Galectins are beta-galactoside-binding animal lectins with conserved carbohydrate recognition domains. The galectins have been implicated in many essential functions including development, differentiation, cell-cell adhesion, cell-matrix interaction, growth regulation, apoptosis, and RNA splicing. This gene is widely expressed in tumoral tissues and seems to be involved in integrin-like cell interactions. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

Known Variants28 total

rsidPosition (GRCh37)AllelesClassClinVar
rs46596821:236,682,248A/Gdownstream gene variant—
rs5507349691:236,687,504C/Tcoding sequence variant—
rs8194141:236,694,232G/Aintron variant—
rs754166581:236,701,105T/Adownstream gene variant—
rs24721221:236,701,359C/G——
rs342999881:236,701,748C/G——
rs25270992381:236,702,226A/T—uncertain significance
rs1512018381:236,702,250G/T—uncertain significance
rs7769965261:236,702,262C/T—uncertain significance
rs7625450351:236,702,263C/T—likely benign
rs1488543121:236,702,360G/T—uncertain significance
rs668771171:236,702,882G/Adownstream gene variant—
rs25271105561:236,703,874A/G—uncertain significance
rs9504206631:236,703,877G/T—uncertain significance
rs7627852121:236,703,909G/A—likely benign
rs3691746481:236,703,971T/G—uncertain significance
rs359684351:236,706,234A/G—benign
rs7548868031:236,706,248G/A—uncertain significance
rs11664734001:236,706,279A/G—likely benign
rs1142140131:236,706,913C/T—benign
rs5554561641:236,706,917G/A—likely benign
rs2020844461:236,706,923G/A—uncertain significance
rs13285983911:236,708,207T/C—uncertain significance
rs7734312281:236,711,325G/A—uncertain significance
rs25271609781:236,711,354A/G—uncertain significance
rs7471819711:236,711,360G/A—uncertain significance
rs5585366061:236,711,372G/C—uncertain significance
rs12727654361:236,711,454G/A—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.