HECW1
HECT, C2 and WW domain containing E3 ubiquitin protein ligase 1
Summary
Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in regulation of dendrite morphogenesis and ubiquitin-dependent protein catabolic process. Predicted to be located in cytosol. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants85 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2024125 | 7:43,158,477 | G/C | — | — |
| rs528092816 | 7:43,267,791 | C/T | — | — |
| rs184603716 | 7:43,285,685 | G/A | intron variant | — |
| rs17172185 | 7:43,286,839 | T/C | intron variant | — |
| rs754996920 | 7:43,351,480 | A/G | — | uncertain significance |
| rs2486024668 | 7:43,351,578 | A/G | — | uncertain significance |
| rs748846572 | 7:43,360,272 | C/T | — | uncertain significance |
| rs17172199 | 7:43,377,276 | A/C | intron variant | — |
| rs543387342 | 7:43,389,652 | G/T | — | — |
| rs540865392 | 7:43,400,571 | G/A | — | uncertain significance |
| rs1404760029 | 7:43,436,461 | C/T | — | uncertain significance |
| rs779347290 | 7:43,436,462 | G/A | — | uncertain significance |
| rs2536403913 | 7:43,447,263 | C/G | — | uncertain significance |
| rs2536645984 | 7:43,477,614 | G/A | — | uncertain significance |
| rs745988614 | 7:43,477,632 | G/A | — | uncertain significance |
| rs756127374 | 7:43,477,671 | C/T | — | uncertain significance |
| rs2536646998 | 7:43,477,701 | C/G | — | uncertain significance |
| rs2536685451 | 7:43,482,145 | A/G | — | uncertain significance |
| rs550586127 | 7:43,482,156 | C/T | — | uncertain significance |
| rs747436165 | 7:43,483,945 | A/G | — | uncertain significance |
| rs767183351 | 7:43,483,984 | C/A | — | uncertain significance |
| rs756487834 | 7:43,484,164 | G/C | — | uncertain significance |
| rs1214501762 | 7:43,484,269 | G/A | — | uncertain significance |
| rs560179850 | 7:43,484,276 | A/G | — | uncertain significance |
| rs889318847 | 7:43,484,300 | G/A | — | likely benign |
| rs561111194 | 7:43,484,321 | A/C | — | uncertain significance |
| rs2076992392 | 7:43,484,394 | G/C | — | uncertain significance |
| rs765678377 | 7:43,484,431 | G/A | — | uncertain significance |
| rs1323812313 | 7:43,484,497 | G/T | — | uncertain significance |
| rs2536710704 | 7:43,484,501 | G/T | — | uncertain significance |
| rs1033513576 | 7:43,484,502 | C/A | — | uncertain significance |
| rs867994249 | 7:43,484,530 | G/A | — | uncertain significance |
| rs200427298 | 7:43,484,591 | C/T | — | uncertain significance |
| rs377717656 | 7:43,484,600 | C/A | — | uncertain significance |
| rs1375648508 | 7:43,484,629 | C/T | — | uncertain significance |
| rs144554534 | 7:43,484,632 | G/A | — | uncertain significance |
| rs1196124919 | 7:43,484,705 | C/G | — | uncertain significance |
| rs2536715208 | 7:43,484,746 | G/A | — | uncertain significance |
| rs370448181 | 7:43,484,789 | G/A | — | uncertain significance |
| rs778008391 | 7:43,484,803 | T/C | — | uncertain significance |
| rs373899022 | 7:43,484,812 | T/A | — | uncertain significance |
| rs147766038 | 7:43,484,823 | C/T | — | benign |
| rs761608981 | 7:43,484,911 | G/A | — | uncertain significance |
| rs2077018483 | 7:43,484,954 | C/T | — | uncertain significance |
| rs201575281 | 7:43,484,988 | G/C | — | likely benign |
| rs2077024540 | 7:43,485,091 | G/A | — | uncertain significance |
| rs373326288 | 7:43,485,103 | G/A | — | uncertain significance |
| rs765564136 | 7:43,490,507 | A/G | — | uncertain significance |
| rs761870097 | 7:43,495,970 | C/T | — | uncertain significance |
| rs779442609 | 7:43,495,977 | C/T | — | uncertain significance |
| rs768975353 | 7:43,503,294 | G/T | — | uncertain significance |
| rs2536873133 | 7:43,503,363 | G/A | — | uncertain significance |
| rs759213624 | 7:43,503,377 | G/A | — | uncertain significance |
| rs767085890 | 7:43,506,115 | C/T | — | uncertain significance |
| rs1192815353 | 7:43,508,588 | C/T | — | uncertain significance |
| rs199913481 | 7:43,508,607 | A/G | — | uncertain significance |
| rs1392964735 | 7:43,508,613 | A/G | — | uncertain significance |
| rs752606904 | 7:43,508,616 | G/A | — | uncertain significance |
| rs374098288 | 7:43,508,688 | C/T | — | uncertain significance |
| rs373090671 | 7:43,508,699 | G/A | — | uncertain significance |
| rs2536924266 | 7:43,508,703 | A/G | — | uncertain significance |
| rs374489291 | 7:43,519,279 | G/A | — | uncertain significance |
| rs368011857 | 7:43,519,284 | C/G | — | uncertain significance |
| rs772084994 | 7:43,519,307 | G/C | — | uncertain significance |
| rs969139600 | 7:43,531,687 | C/G | — | uncertain significance |
| rs2152919693 | 7:43,532,709 | C/T | — | uncertain significance |
| rs754704016 | 7:43,540,335 | G/A | — | uncertain significance |
| rs1333176777 | 7:43,540,369 | T/C | — | uncertain significance |
| rs1350618423 | 7:43,546,744 | A/G | — | uncertain significance |
| rs755869012 | 7:43,546,850 | A/G | — | uncertain significance |
| rs200076235 | 7:43,547,628 | G/A | — | uncertain significance |
| rs1438880550 | 7:43,547,698 | C/A | — | uncertain significance |
| rs61756578 | 7:43,580,774 | C/T | — | likely benign |
| rs991870419 | 7:43,580,793 | G/T | — | uncertain significance |
| rs1366110534 | 7:43,590,146 | G/A | — | uncertain significance |
| rs56111512 | 7:43,591,832 | G/A | — | benign |
| rs4724220 | 7:43,591,955 | G/A | — | benign |
| rs79655368 | 7:43,594,185 | G/A | — | benign |
| rs113348394 | 7:43,594,195 | C/T | — | benign |
| rs1299000474 | 7:43,594,201 | T/A | — | uncertain significance |
| rs139970379 | 7:43,594,218 | G/A | — | uncertain significance |
| rs756422420 | 7:43,594,242 | G/A | — | uncertain significance |
| rs12702051 | 7:43,599,488 | C/T | regulatory region variant | — |
| rs761201866 | 7:43,601,440 | A/G | — | uncertain significance |
| rs2082219898 | 7:43,601,502 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.