IP6K3
inositol hexakisphosphate kinase 3
Summary
This gene encodes a protein that belongs to the inositol phosphokinase (IPK) family. This protein is likely responsible for the conversion of inositol hexakisphosphate (InsP6) to diphosphoinositol pentakisphosphate (InsP7/PP-InsP5). It may also convert 1,3,4,5,6-pentakisphosphate (InsP5) to PP-InsP4. Alternative splicing results in multiple transcript variants encoding the same protein.[provided by RefSeq, Dec 2008]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs748608668 | 6:33,690,633 | C/T | — | uncertain significance |
| rs146926476 | 6:33,690,634 | G/A | — | uncertain significance |
| rs36101795 | 6:33,690,691 | C/T | missense variant | — |
| rs370657692 | 6:33,690,741 | T/C | — | uncertain significance |
| rs778400529 | 6:33,690,744 | A/G | — | uncertain significance |
| rs367580292 | 6:33,690,751 | G/C | — | uncertain significance |
| rs771186925 | 6:33,690,811 | G/C | — | uncertain significance |
| rs758519226 | 6:33,690,817 | G/C | — | uncertain significance |
| rs2533249885 | 6:33,690,828 | G/T | — | uncertain significance |
| rs770106533 | 6:33,690,841 | C/T | — | uncertain significance |
| rs199514412 | 6:33,690,846 | C/T | — | uncertain significance |
| rs767577451 | 6:33,693,226 | C/G | — | uncertain significance |
| rs779209480 | 6:33,693,246 | C/T | — | uncertain significance |
| rs751301300 | 6:33,693,307 | C/A | — | uncertain significance |
| rs145073660 | 6:33,693,357 | G/A | — | uncertain significance |
| rs367942403 | 6:33,694,513 | C/T | — | uncertain significance |
| rs576578939 | 6:33,694,532 | C/T | — | uncertain significance |
| rs746168984 | 6:33,694,543 | C/T | — | uncertain significance |
| rs1411406037 | 6:33,694,580 | G/T | — | uncertain significance |
| rs1766132135 | 6:33,694,582 | T/C | — | uncertain significance |
| rs963523797 | 6:33,694,654 | G/A | — | uncertain significance |
| rs146845617 | 6:33,695,880 | G/T | — | uncertain significance |
| rs561613329 | 6:33,695,917 | G/T | — | uncertain significance |
| rs141588840 | 6:33,695,919 | C/T | — | uncertain significance |
| rs751829854 | 6:33,696,065 | A/G | — | uncertain significance |
| rs114531175 | 6:33,702,938 | C/T | intron variant | — |
| rs757292142 | 6:33,703,090 | G/A | — | uncertain significance |
| rs1197465221 | 6:33,703,147 | T/C | — | uncertain significance |
| rs142228010 | 6:33,703,163 | C/T | — | uncertain significance |
| rs201114812 | 6:33,703,178 | C/T | — | uncertain significance |
| rs140402994 | 6:33,703,208 | C/T | — | uncertain significance |
| rs141301327 | 6:33,703,226 | C/T | — | uncertain significance |
| rs9348924 | 6:33,705,436 | A/G | intron variant | — |
| rs9469578 | 6:33,706,479 | C/A | — | — |
| rs146724774 | 6:33,708,814 | G/A | regulatory region variant | — |
| rs9469582 | 6:33,715,939 | A/G | upstream gene variant | — |
| rs28607030 | 6:33,716,716 | A/G | upstream gene variant | — |
| rs576969883 | 6:33,725,051 | C/A | — | — |
| rs188566407 | 6:33,728,714 | A/T | intergenic variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.