AK8
adenylate kinase 8
Summary
Enables AMP binding activity and nucleobase-containing compound kinase activity. Predicted to be involved in nucleoside monophosphate phosphorylation. Predicted to act upstream of or within ventricular system development. Located in 9+2 motile cilium. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants54 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs200678908 | 9:135,601,109 | C/T | — | uncertain significance |
| rs747724625 | 9:135,601,300 | C/A | — | uncertain significance |
| rs1172663381 | 9:135,602,899 | A/G | — | likely benign |
| rs189965479 | 9:135,616,100 | C/A | — | — |
| rs11243897 | 9:135,618,283 | A/G | intron variant | — |
| rs146699033 | 9:135,628,897 | G/T | intron variant | — |
| rs12552369 | 9:135,632,493 | G/A | intron variant | — |
| rs146561042 | 9:135,646,636 | G/T | upstream gene variant | — |
| rs10901212 | 9:135,647,021 | C/A | upstream gene variant | — |
| rs149828271 | 9:135,648,129 | A/T | upstream gene variant | — |
| rs562713915 | 9:135,649,885 | G/A | — | — |
| rs148798024 | 9:135,654,518 | C/T | intron variant | — |
| rs779035517 | 9:135,668,028 | G/T | — | uncertain significance |
| rs147022583 | 9:135,668,042 | C/T | — | uncertain significance |
| rs769228074 | 9:135,668,064 | C/T | — | uncertain significance |
| rs946535640 | 9:135,668,072 | C/T | — | uncertain significance |
| rs752435497 | 9:135,668,082 | C/T | — | uncertain significance |
| rs571914245 | 9:135,668,085 | G/A | — | uncertain significance |
| rs2540179788 | 9:135,668,111 | T/C | — | uncertain significance |
| rs1209055789 | 9:135,668,119 | G/T | — | uncertain significance |
| rs141905508 | 9:135,668,154 | T/C | — | uncertain significance |
| rs2540180124 | 9:135,668,162 | A/G | — | uncertain significance |
| rs1030833830 | 9:135,690,045 | A/C | — | uncertain significance |
| rs1841728248 | 9:135,698,639 | T/C | — | uncertain significance |
| rs771940681 | 9:135,698,654 | G/A | — | uncertain significance |
| rs1179521659 | 9:135,698,688 | C/T | — | uncertain significance |
| rs753799831 | 9:135,702,253 | C/T | — | uncertain significance |
| rs749270554 | 9:135,702,264 | G/T | — | uncertain significance |
| rs768142703 | 9:135,702,307 | G/A | — | uncertain significance |
| rs1003773855 | 9:135,702,342 | A/T | — | uncertain significance |
| rs76129965 | 9:135,702,354 | G/A | — | uncertain significance |
| rs370809704 | 9:135,702,391 | G/A | — | uncertain significance |
| rs750120409 | 9:135,702,409 | C/T | — | uncertain significance |
| rs183787418 | 9:135,703,415 | C/T | — | uncertain significance |
| rs768761114 | 9:135,703,441 | A/C | — | uncertain significance |
| rs549084019 | 9:135,707,290 | T/C | — | — |
| rs944028 | 9:135,709,381 | T/C | intron variant | — |
| rs773290255 | 9:135,730,272 | C/T | — | uncertain significance |
| rs547319863 | 9:135,730,299 | G/A | — | uncertain significance |
| rs1044389738 | 9:135,730,308 | A/G | — | uncertain significance |
| rs144590872 | 9:135,737,130 | A/G | intron variant | — |
| rs368763451 | 9:135,739,098 | A/C | — | uncertain significance |
| rs529729315 | 9:135,739,099 | A/T | — | uncertain significance |
| rs781746916 | 9:135,739,134 | C/T | — | likely benign |
| rs748022134 | 9:135,739,164 | G/C | — | uncertain significance |
| rs2285938 | 9:135,739,214 | C/T | intron variant | — |
| rs115599655 | 9:135,742,311 | C/T | — | uncertain significance |
| rs748953503 | 9:135,750,511 | T/C | — | uncertain significance |
| rs1193843045 | 9:135,750,514 | C/G | — | uncertain significance |
| rs771154027 | 9:135,750,553 | C/T | — | likely benign |
| rs779143686 | 9:135,753,608 | G/C | — | uncertain significance |
| rs370307434 | 9:135,753,609 | G/T | — | uncertain significance |
| rs761499555 | 9:135,753,618 | G/A | — | uncertain significance |
| rs143313005 | 9:135,753,633 | T/C | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.