STK40
serine/threonine kinase 40
Summary
Predicted to enable ATP binding activity; protein serine kinase activity; and protein serine/threonine kinase activity. Predicted to be involved in regulation of MAPK cascade. Predicted to act upstream of or within several processes, including glycogen metabolic process; lung development; and respiratory system process. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs575657248 | 1:36,807,429 | C/T | — | uncertain significance |
| rs755305561 | 1:36,807,444 | G/T | — | uncertain significance |
| rs200773119 | 1:36,807,451 | C/T | — | uncertain significance |
| rs765322359 | 1:36,807,466 | G/T | — | uncertain significance |
| rs756696476 | 1:36,807,508 | C/G | — | uncertain significance |
| rs56405327 | 1:36,807,563 | C/T | — | benign |
| rs747236810 | 1:36,809,501 | C/T | — | likely benign |
| rs1200783623 | 1:36,809,513 | G/A | — | uncertain significance |
| rs56317061 | 1:36,809,726 | A/G | — | benign |
| rs199920883 | 1:36,809,737 | C/T | — | uncertain significance |
| rs949864906 | 1:36,809,862 | C/T | — | uncertain significance |
| rs1430198106 | 1:36,819,971 | T/C | — | uncertain significance |
| rs182214010 | 1:36,820,917 | C/T | — | uncertain significance |
| rs145965967 | 1:36,820,939 | A/G | — | likely benign |
| rs1171838543 | 1:36,821,030 | C/T | — | uncertain significance |
| rs1475713609 | 1:36,823,843 | G/T | — | uncertain significance |
| rs772996133 | 1:36,823,851 | C/T | — | uncertain significance |
| rs373166224 | 1:36,823,877 | G/A | — | uncertain significance |
| rs747619342 | 1:36,823,931 | C/T | — | uncertain significance |
| rs749056673 | 1:36,823,942 | G/C | — | uncertain significance |
| rs139830713 | 1:36,824,348 | T/C | — | uncertain significance |
| rs757202250 | 1:36,824,369 | T/C | — | uncertain significance |
| rs139903300 | 1:36,824,370 | T/G | — | uncertain significance |
| rs547574448 | 1:36,824,375 | G/A | — | uncertain significance |
| rs201394626 | 1:36,826,893 | G/A | — | uncertain significance |
| rs199672018 | 1:36,826,908 | C/T | — | uncertain significance |
| rs140952107 | 1:36,829,042 | A/T | intron variant | — |
| rs566921175 | 1:36,833,096 | G/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.