METTL25B

methyltransferase like 25B

Summary

Predicted to enable rRNA (adenine-N6,N6-)-dimethyltransferase activity. Predicted to be involved in rRNA methylation. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants36 total

rsidPosition (GRCh37)AllelesClassClinVar
rs2006857431:156,698,943A/Guncertain significance
rs1393892571:156,698,979A/Guncertain significance
rs121457431:156,700,651T/Gupstream gene variant
rs1450082231:156,701,804T/Cuncertain significance
rs7550141681:156,701,807G/Cuncertain significance
rs3686621061:156,702,198G/Auncertain significance
rs7565108061:156,702,215C/Tuncertain significance
rs1181168671:156,702,216G/Auncertain significance
rs7542039791:156,702,218A/Guncertain significance
rs8892756671:156,702,796A/Guncertain significance
rs3678205081:156,702,825G/Auncertain significance
rs1464778921:156,703,207G/Tuncertain significance
rs25250531451:156,703,244G/Auncertain significance
rs5698297751:156,703,820G/Auncertain significance
rs1468181491:156,703,837G/Auncertain significance
rs2015146431:156,703,854C/Auncertain significance
rs25250604551:156,703,880T/Cuncertain significance
rs3691027671:156,703,915C/Guncertain significance
rs1411536541:156,703,916G/Auncertain significance
rs16495219281:156,703,931G/Auncertain significance
rs8892096891:156,703,948G/Auncertain significance
rs3740513201:156,703,961C/Guncertain significance
rs7619538211:156,704,086T/Cuncertain significance
rs7775984121:156,704,108G/Auncertain significance
rs7720470481:156,704,128C/Guncertain significance
rs3734749271:156,704,181C/Guncertain significance
rs5310737421:156,704,188C/Guncertain significance
rs7764713191:156,704,215C/Tuncertain significance
rs7596856941:156,704,222G/Alikely benign
rs7542551911:156,704,236C/Guncertain significance
rs7686505261:156,704,258C/Auncertain significance
rs618135571:156,704,613G/Adownstream gene variant
rs14560031001:156,705,573T/Cuncertain significance
rs7633305361:156,705,677C/Tuncertain significance
rs412674171:156,706,024C/Tdownstream gene variant
rs3721960501:156,706,438C/Tuncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.