ENO4
enolase 4
Summary
Predicted to enable phosphopyruvate hydratase activity. Predicted to be involved in glycolytic process. Predicted to act upstream of or within cilium organization and flagellated sperm motility. Predicted to be located in sperm principal piece. Predicted to be part of phosphopyruvate hydratase complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs555277881 | 10:118,609,118 | G/C | — | uncertain significance |
| rs780545121 | 10:118,609,142 | A/G | — | uncertain significance |
| rs1167802440 | 10:118,609,189 | G/A | — | uncertain significance |
| rs772187861 | 10:118,609,227 | C/A | — | uncertain significance |
| rs2493754839 | 10:118,609,229 | T/C | — | uncertain significance |
| rs1288567606 | 10:118,615,170 | A/C | — | uncertain significance |
| rs2493773411 | 10:118,615,180 | T/C | — | uncertain significance |
| rs1186952659 | 10:118,616,006 | G/A | — | likely benign |
| rs898007360 | 10:118,616,096 | G/A | — | uncertain significance |
| rs7083543 | 10:118,616,110 | C/T | intron variant | — |
| rs781463624 | 10:118,616,136 | C/T | — | uncertain significance |
| rs1040690434 | 10:118,616,162 | T/C | — | uncertain significance |
| rs776738848 | 10:118,618,508 | T/C | — | uncertain significance |
| rs368025714 | 10:118,618,511 | G/A | — | uncertain significance |
| rs759636926 | 10:118,618,548 | T/C | — | uncertain significance |
| rs551253938 | 10:118,620,355 | G/C | — | uncertain significance |
| rs1846390265 | 10:118,620,370 | G/A | — | uncertain significance |
| rs1212682982 | 10:118,620,386 | G/A | — | uncertain significance |
| rs2493786058 | 10:118,620,412 | G/C | — | uncertain significance |
| rs189147503 | 10:118,622,239 | C/A | intron variant | — |
| rs780394520 | 10:118,622,316 | G/A | — | uncertain significance |
| rs9421249 | 10:118,623,322 | C/T | intron variant | — |
| rs185815146 | 10:118,623,580 | G/A | intron variant | — |
| rs1444231260 | 10:118,628,192 | G/A | — | uncertain significance |
| rs918076143 | 10:118,630,645 | A/T | — | uncertain significance |
| rs751411499 | 10:118,630,676 | C/T | — | uncertain significance |
| rs1846687443 | 10:118,630,733 | A/G | — | uncertain significance |
| rs1472199278 | 10:118,633,633 | C/T | — | uncertain significance |
| rs201860890 | 10:118,635,689 | C/T | — | benign |
| rs1477885956 | 10:118,635,766 | T/C | — | uncertain significance |
| rs1271694845 | 10:118,638,815 | C/G | — | uncertain significance |
| rs139862664 | 10:118,639,100 | C/G | downstream gene variant | — |
| rs1404776625 | 10:118,639,399 | G/A | — | uncertain significance |
| rs1043095596 | 10:118,639,409 | G/C | — | uncertain significance |
| rs768037520 | 10:118,639,450 | A/G | — | uncertain significance |
| rs1185737561 | 10:118,639,453 | G/A | — | uncertain significance |
| rs747390021 | 10:118,639,455 | C/T | — | uncertain significance |
| rs896049022 | 10:118,639,464 | A/G | — | uncertain significance |
| rs1286725047 | 10:118,639,486 | A/G | — | uncertain significance |
| rs953823932 | 10:118,641,047 | T/C | — | uncertain significance |
| rs2133286684 | 10:118,641,088 | C/T | — | uncertain significance |
| rs1025931260 | 10:118,641,139 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.