SYPL2
synaptophysin like 2
Summary
Involved in substantia nigra development. Predicted to be located in membrane and synaptic vesicle. Predicted to be active in synaptic vesicle membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants22 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs4970765 | 1:110,009,171 | C/T | regulatory region variant | — |
| rs970767513 | 1:110,009,476 | C/T | — | uncertain significance |
| rs367559384 | 1:110,009,705 | C/T | — | uncertain significance |
| rs10857788 | 1:110,012,289 | G/C | — | — |
| rs114000319 | 1:110,014,465 | A/T | intron variant | — |
| rs776347036 | 1:110,018,204 | T/C | — | uncertain significance |
| rs192895878 | 1:110,018,266 | C/T | — | uncertain significance |
| rs372720702 | 1:110,019,405 | C/T | — | uncertain significance |
| rs532293091 | 1:110,019,406 | G/A | — | uncertain significance |
| rs1656011325 | 1:110,019,423 | C/T | — | uncertain significance |
| rs62623713 | 1:110,019,439 | A/G | missense variant | — |
| rs764541999 | 1:110,019,475 | T/A | — | uncertain significance |
| rs376768412 | 1:110,019,555 | C/T | — | uncertain significance |
| rs867305380 | 1:110,019,565 | A/C | — | uncertain significance |
| rs760834976 | 1:110,019,578 | G/A | — | likely benign |
| rs993888687 | 1:110,020,453 | C/T | — | uncertain significance |
| rs757240709 | 1:110,020,485 | G/A | — | uncertain significance |
| rs1346239668 | 1:110,020,524 | G/A | — | uncertain significance |
| rs9661614 | 1:110,021,837 | T/C | regulatory region variant | — |
| rs772348390 | 1:110,022,073 | G/A | — | uncertain significance |
| rs115819583 | 1:110,022,940 | A/G | upstream gene variant | — |
| rs485660 | 1:110,023,432 | G/A | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.