STYXL1
serine/threonine/tyrosine interacting like 1
Summary
Enables protein phosphatase binding activity and pseudophosphatase activity. Involved in negative regulation of stress granule assembly; positive regulation of intrinsic apoptotic signaling pathway; and positive regulation of neuron projection development. Located in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants27 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs150015474 | 7:75,625,797 | G/C | — | benign |
| rs1248440869 | 7:75,625,814 | A/G | — | uncertain significance |
| rs139867483 | 7:75,625,840 | C/G | — | uncertain significance |
| rs2060222358 | 7:75,625,860 | C/T | — | uncertain significance |
| rs142991497 | 7:75,630,252 | C/T | — | likely benign |
| rs868977743 | 7:75,630,254 | G/T | — | uncertain significance |
| rs377455963 | 7:75,630,264 | G/A | — | uncertain significance |
| rs1554566948 | 7:75,630,266 | C/G | — | uncertain significance |
| rs149776933 | 7:75,633,096 | C/T | — | uncertain significance |
| rs2535516615 | 7:75,633,114 | T/C | — | uncertain significance |
| rs1044484 | 7:75,634,687 | A/G | — | benign |
| rs569304621 | 7:75,635,162 | A/G | — | — |
| rs1554572948 | 7:75,643,062 | G/C | — | uncertain significance |
| rs782646288 | 7:75,643,103 | G/A | — | likely benign |
| rs1792918926 | 7:75,643,185 | T/C | — | uncertain significance |
| rs367788597 | 7:75,643,197 | G/A | — | uncertain significance |
| rs1181080046 | 7:75,651,204 | T/A | — | uncertain significance |
| rs782227909 | 7:75,651,205 | C/T | — | uncertain significance |
| rs61740075 | 7:75,651,253 | C/T | — | uncertain significance |
| rs895564431 | 7:75,651,295 | G/A | — | uncertain significance |
| rs58925536 | 7:75,654,574 | C/G | — | — |
| rs113570449 | 7:75,654,977 | G/T | — | — |
| rs78478514 | 7:75,655,896 | C/T | intron variant | — |
| rs148066291 | 7:75,658,000 | T/C | — | uncertain significance |
| rs145942606 | 7:75,659,753 | T/C | — | likely benign |
| rs28446604 | 7:75,662,518 | C/T | intron variant | — |
| rs61303167 | 7:75,671,175 | G/T | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.