HYKK
hydroxylysine kinase
Summary
Enables hydroxylysine kinase activity. Predicted to be involved in lysine catabolic process. Predicted to be located in mitochondrial matrix. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7168796 | 15:78,800,494 | C/G | — | — |
| rs11852372 | 15:78,801,394 | A/C | intron variant | — |
| rs7164594 | 15:78,803,057 | C/A | — | — |
| rs372264847 | 15:78,805,456 | C/T | — | uncertain significance |
| rs377660640 | 15:78,805,584 | G/A | — | likely benign |
| rs767395546 | 15:78,805,603 | G/A | — | uncertain significance |
| rs2052095208 | 15:78,805,720 | C/T | — | uncertain significance |
| rs8034191 | 15:78,806,023 | T/C | intron variant | pathogenic |
| rs929860582 | 15:78,807,349 | T/C | — | uncertain significance |
| rs1256839159 | 15:78,807,360 | C/T | — | uncertain significance |
| rs762296061 | 15:78,807,381 | C/A | — | likely benign |
| rs766699103 | 15:78,807,403 | T/C | — | uncertain significance |
| rs751013035 | 15:78,807,417 | A/G | — | uncertain significance |
| rs28437878 | 15:78,807,872 | C/T | intron variant | — |
| rs12438181 | 15:78,812,098 | G/T | — | — |
| rs12441426 | 15:78,812,329 | T/C | intron variant | — |
| rs34684276 | 15:78,813,155 | G/A | intron variant | — |
| rs10519203 | 15:78,814,046 | G/A | intron variant | — |
| rs61204066 | 15:78,815,298 | G/A | intron variant | — |
| rs8031948 | 15:78,816,057 | G/T | intron variant | — |
| rs2542678056 | 15:78,819,766 | C/G | — | uncertain significance |
| rs760694142 | 15:78,819,785 | G/A | — | uncertain significance |
| rs200988294 | 15:78,819,849 | A/G | — | uncertain significance |
| rs1251283478 | 15:78,819,864 | T/A | — | uncertain significance |
| rs12441354 | 15:78,821,016 | G/A | intron variant | — |
| rs7169584 | 15:78,822,660 | A/C | — | — |
| rs12915428 | 15:78,823,368 | G/A | intron variant | — |
| rs1847530 | 15:78,824,031 | G/A | intron variant | — |
| rs12438659 | 15:78,824,924 | G/T | — | — |
| rs767707878 | 15:78,825,608 | G/A | — | uncertain significance |
| rs1324664822 | 15:78,825,609 | C/T | — | uncertain significance |
| rs756658354 | 15:78,825,654 | G/T | — | uncertain significance |
| rs754287771 | 15:78,825,664 | C/G | — | uncertain significance |
| rs2542684477 | 15:78,825,716 | G/A | — | uncertain significance |
| rs1297974168 | 15:78,825,759 | G/A | — | uncertain significance |
| rs1567025803 | 15:78,825,893 | A/C | — | uncertain significance |
| rs931794 | 15:78,826,180 | G/C | — | — |
| rs2036534 | 15:78,826,948 | T/A | — | — |
| rs28675338 | 15:78,827,631 | C/T | — | — |
| rs12439240 | 15:78,829,091 | T/C | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.