ESYT3
extended synaptotagmin 3
Summary
Predicted to enable calcium ion binding activity and phospholipid binding activity. Predicted to be involved in endoplasmic reticulum-plasma membrane tethering and lipid transport. Located in cytoplasmic side of plasma membrane; endoplasmic reticulum membrane; and endoplasmic reticulum-plasma membrane contact site. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants61 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs377514411 | 3:138,153,668 | G/T | — | uncertain significance |
| rs2030508494 | 3:138,153,707 | C/A | — | uncertain significance |
| rs759716021 | 3:138,153,858 | G/T | — | uncertain significance |
| rs191240658 | 3:138,153,923 | G/A | missense variant | — |
| rs769401642 | 3:138,153,951 | A/T | — | likely benign |
| rs10513053 | 3:138,154,363 | C/T | regulatory region variant | — |
| rs1109088 | 3:138,154,795 | G/T | — | — |
| rs4678419 | 3:138,172,015 | C/T | intron variant | — |
| rs570708059 | 3:138,174,043 | C/T | — | uncertain significance |
| rs773424184 | 3:138,174,087 | C/T | — | uncertain significance |
| rs114454261 | 3:138,174,127 | A/C | — | uncertain significance |
| rs766107080 | 3:138,176,411 | G/A | — | uncertain significance |
| rs757233859 | 3:138,176,447 | C/T | — | uncertain significance |
| rs2474269694 | 3:138,179,484 | A/G | — | uncertain significance |
| rs749114663 | 3:138,179,485 | C/A | — | uncertain significance |
| rs151078027 | 3:138,179,493 | A/C | — | uncertain significance |
| rs201949984 | 3:138,179,496 | C/T | — | uncertain significance |
| rs112771629 | 3:138,180,965 | A/G | — | likely benign |
| rs941155548 | 3:138,180,986 | C/T | — | uncertain significance |
| rs145754623 | 3:138,181,028 | C/A | — | uncertain significance |
| rs201784871 | 3:138,183,296 | A/G | — | uncertain significance |
| rs376528570 | 3:138,183,305 | G/A | — | uncertain significance |
| rs1418984773 | 3:138,184,223 | C/G | — | uncertain significance |
| rs767978186 | 3:138,184,249 | T/A | — | uncertain significance |
| rs565978929 | 3:138,186,414 | G/A | — | uncertain significance |
| rs765784956 | 3:138,186,989 | C/T | — | uncertain significance |
| rs747086756 | 3:138,187,034 | G/A | — | uncertain significance |
| rs147129542 | 3:138,187,527 | G/A | — | uncertain significance |
| rs780457274 | 3:138,188,313 | A/T | — | uncertain significance |
| rs945378874 | 3:138,188,331 | G/C | — | uncertain significance |
| rs375983343 | 3:138,188,956 | C/T | — | uncertain significance |
| rs767624112 | 3:138,188,960 | A/G | — | likely benign |
| rs1436399512 | 3:138,188,965 | G/A | — | uncertain significance |
| rs372182457 | 3:138,189,764 | C/T | — | uncertain significance |
| rs1367243594 | 3:138,189,797 | A/G | — | uncertain significance |
| rs747948570 | 3:138,189,809 | C/T | — | uncertain significance |
| rs1208471331 | 3:138,189,819 | T/C | — | uncertain significance |
| rs2033189065 | 3:138,189,822 | A/G | — | uncertain significance |
| rs774470802 | 3:138,189,831 | G/A | — | uncertain significance |
| rs764669605 | 3:138,189,866 | C/T | — | uncertain significance |
| rs373793480 | 3:138,191,224 | G/A | — | uncertain significance |
| rs868514919 | 3:138,191,245 | C/T | — | uncertain significance |
| rs2474299446 | 3:138,191,278 | T/A | — | uncertain significance |
| rs761602771 | 3:138,191,299 | A/T | — | uncertain significance |
| rs765191108 | 3:138,191,301 | C/G | — | uncertain significance |
| rs1388315337 | 3:138,191,352 | C/A | — | uncertain significance |
| rs199942859 | 3:138,191,382 | G/A | — | uncertain significance |
| rs1326751877 | 3:138,191,390 | G/T | — | uncertain significance |
| rs766286102 | 3:138,191,425 | C/G | — | uncertain significance |
| rs767663447 | 3:138,191,437 | C/T | — | uncertain significance |
| rs2033285895 | 3:138,191,514 | A/G | — | uncertain significance |
| rs563182087 | 3:138,191,526 | A/G | — | uncertain significance |
| rs200613499 | 3:138,191,662 | C/T | — | uncertain significance |
| rs201126281 | 3:138,192,395 | G/A | — | likely benign |
| rs199809846 | 3:138,192,397 | C/T | — | uncertain significance |
| rs756062839 | 3:138,193,077 | G/A | — | uncertain significance |
| rs200647256 | 3:138,193,164 | G/A | — | uncertain significance |
| rs753822960 | 3:138,193,185 | T/C | — | uncertain significance |
| rs2033474050 | 3:138,195,085 | T/C | — | uncertain significance |
| rs371615515 | 3:138,195,103 | G/A | — | uncertain significance |
| rs755120267 | 3:138,195,114 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.