HK3
hexokinase 3
Summary
Hexokinases phosphorylate glucose to produce glucose-6-phosphate, the first step in most glucose metabolism pathways. This gene encodes hexokinase 3. Similar to hexokinases 1 and 2, this allosteric enzyme is inhibited by its product glucose-6-phosphate. [provided by RefSeq, Apr 2009]
Known Variants96 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs150401292 | 5:176,308,081 | C/T | — | uncertain significance |
| rs1413800944 | 5:176,308,112 | C/T | — | uncertain significance |
| rs146153216 | 5:176,308,136 | C/T | — | uncertain significance |
| rs200923960 | 5:176,308,308 | G/C | — | uncertain significance |
| rs1322592654 | 5:176,308,334 | C/T | — | uncertain significance |
| rs1380149933 | 5:176,308,375 | C/T | — | uncertain significance |
| rs755391790 | 5:176,308,376 | G/A | — | uncertain significance |
| rs373687842 | 5:176,308,412 | A/G | — | uncertain significance |
| rs778604405 | 5:176,308,498 | T/C | — | uncertain significance |
| rs2532551248 | 5:176,308,736 | T/C | — | uncertain significance |
| rs61755710 | 5:176,308,737 | C/A | — | uncertain significance |
| rs566539907 | 5:176,308,744 | C/T | — | uncertain significance |
| rs145588665 | 5:176,308,763 | G/A | — | uncertain significance |
| rs569541765 | 5:176,308,772 | C/T | — | uncertain significance |
| rs766958235 | 5:176,308,823 | A/T | — | uncertain significance |
| rs369520286 | 5:176,308,955 | C/T | — | uncertain significance |
| rs78805667 | 5:176,308,984 | G/C | — | benign |
| rs745623940 | 5:176,308,993 | C/T | — | uncertain significance |
| rs35676647 | 5:176,308,995 | G/A | — | benign |
| rs139364608 | 5:176,309,017 | C/T | — | uncertain significance |
| rs371103424 | 5:176,309,022 | G/T | — | uncertain significance |
| rs758880985 | 5:176,309,044 | A/C | — | uncertain significance |
| rs2532552300 | 5:176,309,069 | C/G | — | uncertain significance |
| rs777101167 | 5:176,309,071 | C/T | — | uncertain significance |
| rs372156267 | 5:176,309,072 | C/T | — | uncertain significance |
| rs375907484 | 5:176,309,084 | C/G | — | uncertain significance |
| rs145014783 | 5:176,309,092 | C/T | — | likely benign |
| rs147409752 | 5:176,309,093 | G/A | — | uncertain significance |
| rs2532552494 | 5:176,309,096 | G/A | — | uncertain significance |
| rs1469863578 | 5:176,309,103 | C/G | — | uncertain significance |
| rs691276 | 5:176,309,487 | G/A | — | — |
| rs757892659 | 5:176,310,789 | C/T | — | likely benign |
| rs779271345 | 5:176,310,797 | G/A | — | uncertain significance |
| rs138002696 | 5:176,310,849 | C/T | — | uncertain significance |
| rs778250236 | 5:176,311,071 | C/G | — | uncertain significance |
| rs114856191 | 5:176,311,091 | G/A | — | likely benign |
| rs191550498 | 5:176,312,433 | T/C | downstream gene variant | — |
| rs779857825 | 5:176,314,034 | G/A | — | uncertain significance |
| rs368066219 | 5:176,314,046 | C/T | — | uncertain significance |
| rs140696619 | 5:176,314,065 | C/T | — | uncertain significance |
| rs200906801 | 5:176,314,078 | C/G | — | uncertain significance |
| rs372392371 | 5:176,314,213 | A/G | — | uncertain significance |
| rs778816240 | 5:176,314,231 | C/T | — | uncertain significance |
| rs1412289970 | 5:176,314,233 | G/A | — | uncertain significance |
| rs200480878 | 5:176,314,268 | T/A | — | likely benign |
| rs1228762242 | 5:176,314,315 | C/T | — | uncertain significance |
| rs143577771 | 5:176,314,320 | G/A | — | uncertain significance |
| rs1204803991 | 5:176,314,346 | G/A | — | likely benign |
| rs554872384 | 5:176,314,497 | G/A | — | uncertain significance |
| rs144629628 | 5:176,314,538 | C/T | — | uncertain significance |
| rs142608480 | 5:176,314,560 | C/T | — | uncertain significance |
| rs759109859 | 5:176,314,580 | C/T | — | uncertain significance |
| rs775508008 | 5:176,314,587 | G/A | — | uncertain significance |
| rs376532514 | 5:176,314,614 | G/A | — | uncertain significance |
| rs184900635 | 5:176,314,638 | C/T | — | uncertain significance |
| rs367626464 | 5:176,314,652 | G/T | — | uncertain significance |
| rs1458621297 | 5:176,315,342 | C/T | — | likely benign |
| rs111627568 | 5:176,315,354 | C/T | — | uncertain significance |
| rs755294955 | 5:176,315,442 | A/G | — | uncertain significance |
| rs767209073 | 5:176,315,471 | G/A | — | uncertain significance |
| rs374550151 | 5:176,315,538 | C/T | — | likely benign |
| rs956253223 | 5:176,315,546 | C/T | — | uncertain significance |
| rs369428434 | 5:176,315,752 | C/T | — | uncertain significance |
| rs1309133983 | 5:176,315,765 | G/T | — | uncertain significance |
| rs139187398 | 5:176,315,797 | C/T | — | likely benign |
| rs61740251 | 5:176,316,425 | C/A | — | uncertain significance |
| rs745368895 | 5:176,316,427 | A/C | — | uncertain significance |
| rs35610191 | 5:176,316,455 | T/C | — | not provided |
| rs2532570197 | 5:176,316,457 | T/G | — | uncertain significance |
| rs2532570258 | 5:176,316,477 | C/A | — | uncertain significance |
| rs541590139 | 5:176,316,482 | C/T | — | likely benign |
| rs141772552 | 5:176,316,503 | G/A | — | uncertain significance |
| rs112160979 | 5:176,316,668 | C/T | — | benign |
| rs200190227 | 5:176,316,681 | G/A | — | likely benign |
| rs2532573001 | 5:176,317,652 | G/A | — | uncertain significance |
| rs2532573043 | 5:176,317,666 | C/A | — | uncertain significance |
| rs2532573058 | 5:176,317,674 | C/T | — | uncertain significance |
| rs1561683757 | 5:176,317,713 | T/A | — | uncertain significance |
| rs2532573408 | 5:176,317,823 | C/T | — | uncertain significance |
| rs146251872 | 5:176,317,833 | C/T | — | uncertain significance |
| rs1758747777 | 5:176,317,870 | G/T | — | uncertain significance |
| rs747370923 | 5:176,317,910 | C/G | — | uncertain significance |
| rs147960651 | 5:176,318,086 | G/T | — | uncertain significance |
| rs766901550 | 5:176,318,093 | G/T | — | uncertain significance |
| rs369230456 | 5:176,318,105 | T/C | — | uncertain significance |
| rs1418386309 | 5:176,318,130 | C/T | — | uncertain significance |
| rs996496649 | 5:176,318,135 | A/G | — | uncertain significance |
| rs141892147 | 5:176,318,142 | G/A | — | uncertain significance |
| rs199663371 | 5:176,318,150 | G/A | — | likely benign |
| rs1251348540 | 5:176,318,151 | C/T | — | uncertain significance |
| rs758616907 | 5:176,318,413 | C/A | — | uncertain significance |
| rs1171817495 | 5:176,318,428 | T/G | — | uncertain significance |
| rs61739890 | 5:176,318,430 | C/T | — | benign |
| rs1388211903 | 5:176,318,442 | G/T | — | uncertain significance |
| rs760597997 | 5:176,318,534 | C/A | — | uncertain significance |
| rs1026763733 | 5:176,323,127 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.