KLF17

KLF transcription factor 17

Summary

Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II. Predicted to act upstream of or within gamete generation. Predicted to be located in chromatin. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants34 total

rsidPosition (GRCh37)AllelesClassClinVar
rs66983331:44,554,457C/G
rs2010937551:44,584,641C/Tlikely benign
rs1894642661:44,590,970C/Tupstream gene variant
rs7585673381:44,595,031G/Alikely benign
rs7557306661:44,595,041C/Tuncertain significance
rs25227646081:44,595,068C/Auncertain significance
rs25227648521:44,595,110C/Auncertain significance
rs7554762851:44,595,144G/Tuncertain significance
rs3739896361:44,595,203C/Auncertain significance
rs14475934501:44,595,212G/Tuncertain significance
rs2000139031:44,595,221T/Cuncertain significance
rs20880765911:44,595,224C/Tuncertain significance
rs7800074111:44,595,254C/Tlikely benign
rs7584617141:44,595,316A/Guncertain significance
rs25227669921:44,595,380C/Tuncertain significance
rs7527506061:44,595,403C/Tuncertain significance
rs7776516901:44,595,407C/Guncertain significance
rs7634023281:44,595,482C/Tuncertain significance
rs1432241051:44,595,487C/Tuncertain significance
rs1413070731:44,595,511A/Tuncertain significance
rs13095672631:44,595,637G/Tuncertain significance
rs7469597761:44,595,658C/Tlikely benign
rs20880864671:44,595,675C/Auncertain significance
rs7501852701:44,595,700G/Cuncertain significance
rs2002920261:44,595,709G/Alikely benign
rs1443792571:44,595,743G/Auncertain significance
rs25227696731:44,595,773C/Tuncertain significance
rs7671037841:44,595,814G/Auncertain significance
rs25227723501:44,596,206C/Auncertain significance
rs7743187891:44,596,222T/Cuncertain significance
rs7762400551:44,596,261C/Tuncertain significance
rs25227729611:44,596,328A/Guncertain significance
rs25227733181:44,596,367C/Tuncertain significance
rs5402696151:44,596,402G/Auncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.