KLHL29
kelch like family member 29
Summary
Predicted to enable ubiquitin-like ligase-substrate adaptor activity. Predicted to be involved in proteasome-mediated ubiquitin-dependent protein catabolic process. Predicted to be part of Cul3-RING ubiquitin ligase complex. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants65 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs746934947 | 2:23,785,074 | G/A | — | uncertain significance |
| rs935119633 | 2:23,785,091 | G/A | — | uncertain significance |
| rs1042988239 | 2:23,785,104 | G/A | — | uncertain significance |
| rs373873641 | 2:23,785,133 | G/A | — | uncertain significance |
| rs2465998435 | 2:23,785,149 | G/A | — | uncertain significance |
| rs139637554 | 2:23,785,158 | G/A | — | uncertain significance |
| rs564248042 | 2:23,785,179 | G/C | — | uncertain significance |
| rs985031237 | 2:23,785,184 | G/A | — | uncertain significance |
| rs1416175987 | 2:23,785,191 | G/T | — | uncertain significance |
| rs561931922 | 2:23,785,211 | G/A | — | uncertain significance |
| rs751592288 | 2:23,785,223 | C/T | — | uncertain significance |
| rs757296959 | 2:23,785,251 | G/A | — | uncertain significance |
| rs967941602 | 2:23,785,292 | G/A | — | uncertain significance |
| rs926293779 | 2:23,785,301 | G/A | — | uncertain significance |
| rs1667475692 | 2:23,785,347 | C/A | — | uncertain significance |
| rs143536916 | 2:23,822,075 | C/G | intron variant | — |
| rs2466184340 | 2:23,862,063 | C/T | — | uncertain significance |
| rs747389353 | 2:23,862,076 | C/T | — | uncertain significance |
| rs769232022 | 2:23,862,113 | G/C | — | uncertain significance |
| rs369014829 | 2:23,862,131 | G/A | — | uncertain significance |
| rs772033256 | 2:23,865,276 | G/A | — | uncertain significance |
| rs775388181 | 2:23,865,285 | C/A | — | uncertain significance |
| rs1313847320 | 2:23,865,301 | C/A | — | uncertain significance |
| rs781228421 | 2:23,865,373 | C/T | — | uncertain significance |
| rs553327378 | 2:23,865,406 | C/T | — | uncertain significance |
| rs2466195493 | 2:23,865,432 | G/A | — | uncertain significance |
| rs751666224 | 2:23,865,543 | G/A | — | uncertain significance |
| rs541465243 | 2:23,865,558 | C/A | — | uncertain significance |
| rs547025701 | 2:23,865,625 | A/G | — | uncertain significance |
| rs2466196595 | 2:23,865,639 | A/C | — | uncertain significance |
| rs776374748 | 2:23,865,642 | G/A | — | uncertain significance |
| rs769742318 | 2:23,865,676 | T/C | — | uncertain significance |
| rs200492957 | 2:23,865,678 | G/A | — | uncertain significance |
| rs749985561 | 2:23,865,681 | G/A | — | uncertain significance |
| rs66523860 | 2:23,880,823 | A/G | intron variant | — |
| rs56163696 | 2:23,885,560 | C/T | intron variant | — |
| rs7586023 | 2:23,889,134 | C/A | — | — |
| rs200560025 | 2:23,896,132 | A/G | — | — |
| rs4665630 | 2:23,898,317 | C/G | — | — |
| rs6714016 | 2:23,899,948 | A/G | intron variant | — |
| rs1468878238 | 2:23,907,301 | G/A | — | uncertain significance |
| rs367696673 | 2:23,907,302 | C/T | — | uncertain significance |
| rs202215562 | 2:23,914,544 | G/A | — | likely benign |
| rs368416333 | 2:23,914,548 | G/A | — | uncertain significance |
| rs371850727 | 2:23,914,560 | G/A | — | likely benign |
| rs541560688 | 2:23,914,590 | G/A | — | uncertain significance |
| rs768911245 | 2:23,914,659 | A/G | — | uncertain significance |
| rs748195862 | 2:23,914,668 | G/A | — | uncertain significance |
| rs2465373775 | 2:23,914,713 | C/T | — | uncertain significance |
| rs2465385784 | 2:23,916,139 | A/G | — | uncertain significance |
| rs1316541027 | 2:23,916,239 | G/T | — | uncertain significance |
| rs911194368 | 2:23,916,306 | G/A | — | likely benign |
| rs578019029 | 2:23,918,497 | C/T | — | uncertain significance |
| rs928699381 | 2:23,918,642 | C/A | — | uncertain significance |
| rs771752047 | 2:23,919,302 | G/A | — | uncertain significance |
| rs2465410682 | 2:23,919,371 | A/G | — | uncertain significance |
| rs140516864 | 2:23,926,071 | T/C | — | likely benign |
| rs373265062 | 2:23,926,090 | G/A | — | uncertain significance |
| rs1288198338 | 2:23,926,094 | C/G | — | uncertain significance |
| rs755066901 | 2:23,926,111 | C/T | — | uncertain significance |
| rs1358727996 | 2:23,926,186 | G/A | — | uncertain significance |
| rs1044121142 | 2:23,926,613 | C/G | — | uncertain significance |
| rs2465465220 | 2:23,926,661 | C/T | — | uncertain significance |
| rs887352240 | 2:23,929,413 | C/T | — | uncertain significance |
| rs747900140 | 2:23,929,446 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.