KLF15
KLF transcription factor 15
Summary
Enables DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in negative regulation of peptidyl-lysine acetylation and positive regulation of transcription by RNA polymerase II. Located in nuclear speck. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11718633 | 3:126,012,421 | C/T | downstream gene variant | — |
| rs9811543 | 3:126,038,044 | A/G | intergenic variant | — |
| rs759530999 | 3:126,062,583 | C/A | — | uncertain significance |
| rs1397851303 | 3:126,062,584 | G/T | — | uncertain significance |
| rs201850035 | 3:126,062,593 | G/A | — | uncertain significance |
| rs1481122855 | 3:126,062,627 | C/A | — | uncertain significance |
| rs9838915 | 3:126,066,220 | G/A | intron variant | — |
| rs6796325 | 3:126,068,557 | C/T | intron variant | — |
| rs376424318 | 3:126,070,712 | C/T | — | uncertain significance |
| rs144702822 | 3:126,070,736 | G/A | — | uncertain significance |
| rs760542349 | 3:126,070,801 | T/C | — | uncertain significance |
| rs1560040637 | 3:126,070,814 | T/C | — | uncertain significance |
| rs963005118 | 3:126,070,842 | C/A | — | uncertain significance |
| rs1338386027 | 3:126,070,852 | A/G | — | uncertain significance |
| rs376824998 | 3:126,070,979 | C/T | — | uncertain significance |
| rs961177388 | 3:126,071,041 | G/T | — | uncertain significance |
| rs1352453690 | 3:126,071,042 | C/T | — | uncertain significance |
| rs769683928 | 3:126,071,054 | A/G | — | uncertain significance |
| rs1336716498 | 3:126,071,099 | T/A | — | uncertain significance |
| rs1307742816 | 3:126,071,108 | A/C | — | uncertain significance |
| rs754269546 | 3:126,071,120 | G/A | — | uncertain significance |
| rs148757851 | 3:126,071,176 | C/G | — | uncertain significance |
| rs1009734442 | 3:126,071,194 | C/T | — | uncertain significance |
| rs201547298 | 3:126,071,195 | G/A | — | uncertain significance |
| rs61736553 | 3:126,071,363 | G/A | — | uncertain significance |
| rs375056469 | 3:126,071,396 | C/T | — | uncertain significance |
| rs762587746 | 3:126,071,575 | T/C | — | uncertain significance |
| rs371458343 | 3:126,071,666 | T/C | — | uncertain significance |
| rs371674888 | 3:126,071,678 | G/A | — | uncertain significance |
| rs753392896 | 3:126,071,681 | G/A | — | uncertain significance |
| rs368930877 | 3:126,071,728 | G/A | — | likely benign |
| rs189318146 | 3:126,073,488 | C/T | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.