KLF13
KLF transcription factor 13
Summary
KLF13 belongs to a family of transcription factors that contain 3 classical zinc finger DNA-binding domains consisting of a zinc atom tetrahedrally coordinated by 2 cysteines and 2 histidines (C2H2 motif). These transcription factors bind to GC-rich sequences and related GT and CACCC boxes (Scohy et al., 2000 [PubMed 11087666]).[supplied by OMIM, Mar 2008]
Known Variants49 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2038725860 | 15:31,619,423 | C/T | — | uncertain significance |
| rs77996726 | 15:31,619,442 | C/T | — | benign |
| rs923421633 | 15:31,619,472 | G/A | — | likely benign |
| rs1260495008 | 15:31,619,504 | G/A | — | uncertain significance |
| rs2504084752 | 15:31,619,510 | A/G | — | uncertain significance |
| rs2038728701 | 15:31,619,518 | C/G | — | uncertain significance |
| rs777251052 | 15:31,619,531 | C/T | — | uncertain significance |
| rs997747683 | 15:31,619,542 | A/C | — | uncertain significance |
| rs1057070402 | 15:31,619,548 | A/C | — | uncertain significance |
| rs2038732192 | 15:31,619,611 | C/T | — | uncertain significance |
| rs1018351613 | 15:31,619,654 | C/T | — | uncertain significance |
| rs1030560832 | 15:31,619,698 | C/T | — | uncertain significance |
| rs955143288 | 15:31,619,704 | C/G | — | uncertain significance |
| rs973487036 | 15:31,619,727 | G/C | — | uncertain significance |
| rs1595445500 | 15:31,619,731 | A/C | — | uncertain significance |
| rs1241229922 | 15:31,619,734 | T/C | — | uncertain significance |
| rs1202438054 | 15:31,619,740 | G/C | — | uncertain significance |
| rs937332764 | 15:31,619,741 | G/C | — | uncertain significance |
| rs2038736102 | 15:31,619,743 | G/C | — | uncertain significance |
| rs2038736400 | 15:31,619,747 | A/C | — | uncertain significance |
| rs2038736468 | 15:31,619,748 | A/C | — | uncertain significance |
| rs2504086644 | 15:31,619,752 | G/C | — | uncertain significance |
| rs1253073009 | 15:31,619,779 | T/G | — | uncertain significance |
| rs568489216 | 15:31,619,787 | G/C | — | conflicting classifications of pathogenicity |
| rs1163627771 | 15:31,619,819 | G/A | — | uncertain significance |
| rs1175670418 | 15:31,619,828 | G/A | — | uncertain significance |
| rs1015033557 | 15:31,619,869 | C/A | — | likely benign |
| rs1313605961 | 15:31,619,872 | C/T | — | uncertain significance |
| rs201002318 | 15:31,619,934 | C/T | — | benign |
| rs12439534 | 15:31,621,985 | C/T | — | — |
| rs4779517 | 15:31,636,424 | C/G | intron variant | — |
| rs4779863 | 15:31,636,675 | C/G | intron variant | — |
| rs28510484 | 15:31,637,569 | G/C | regulatory region variant | — |
| rs16956707 | 15:31,641,633 | G/A | intron variant | — |
| rs546099707 | 15:31,660,064 | G/A | — | — |
| rs144180630 | 15:31,664,259 | C/T | — | likely benign |
| rs142865735 | 15:31,664,304 | C/T | — | likely benign |
| rs1487759796 | 15:31,664,334 | G/C | — | uncertain significance |
| rs199626018 | 15:31,664,352 | C/T | — | likely benign |
| rs747606436 | 15:31,664,370 | C/T | — | likely benign |
| rs773950563 | 15:31,664,383 | G/A | — | uncertain significance |
| rs148453619 | 15:31,664,397 | G/A | — | benign |
| rs765496627 | 15:31,664,413 | C/G | — | uncertain significance |
| rs747004379 | 15:31,664,434 | G/A | — | uncertain significance |
| rs761962587 | 15:31,664,457 | C/T | — | likely benign |
| rs8042404 | 15:31,680,016 | G/C | — | — |
| rs4779872 | 15:31,705,409 | A/C | — | — |
| rs79087789 | 15:31,722,199 | G/A | — | — |
| rs969811939 | 15:31,727,723 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.