SNX31
sorting nexin 31
Summary
Predicted to enable phosphatidylinositol binding activity. Predicted to be involved in endocytic recycling and intracellular protein transport. Predicted to be located in cytoskeleton. Predicted to be part of protein-containing complex. Predicted to be active in early endosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs767107523 | 8:101,586,154 | C/T | — | uncertain significance |
| rs2487952216 | 8:101,586,170 | A/T | — | uncertain significance |
| rs749791336 | 8:101,586,181 | T/C | — | uncertain significance |
| rs144166924 | 8:101,589,290 | G/A | — | uncertain significance |
| rs751884188 | 8:101,601,102 | T/C | — | uncertain significance |
| rs2488227644 | 8:101,608,923 | T/G | — | uncertain significance |
| rs989200148 | 8:101,608,970 | A/G | — | uncertain significance |
| rs139602322 | 8:101,609,014 | A/C | — | uncertain significance |
| rs1384790109 | 8:101,609,050 | C/A | — | uncertain significance |
| rs532024545 | 8:101,612,617 | T/C | — | uncertain significance |
| rs762623454 | 8:101,620,777 | G/A | — | uncertain significance |
| rs200656076 | 8:101,625,247 | A/G | — | uncertain significance |
| rs143289856 | 8:101,625,274 | C/T | — | uncertain significance |
| rs760919579 | 8:101,629,870 | T/C | — | uncertain significance |
| rs142883851 | 8:101,629,878 | T/C | — | uncertain significance |
| rs1169647045 | 8:101,629,892 | T/C | — | uncertain significance |
| rs201994033 | 8:101,642,562 | G/A | — | likely benign |
| rs746275000 | 8:101,642,581 | C/T | — | likely benign |
| rs749488970 | 8:101,642,602 | C/A | — | uncertain significance |
| rs745824904 | 8:101,642,607 | G/C | — | uncertain significance |
| rs147376243 | 8:101,661,516 | C/A | — | uncertain significance |
| rs2488684005 | 8:101,661,554 | C/G | — | uncertain significance |
| rs758900796 | 8:101,661,560 | A/G | — | uncertain significance |
| rs1313705428 | 8:101,661,569 | G/C | — | uncertain significance |
| rs1219045664 | 8:101,661,733 | G/A | — | uncertain significance |
| rs1693591 | 8:101,673,265 | T/G | intron variant | — |
| rs3115895 | 8:101,673,915 | A/G | — | — |
| rs2978098 | 8:101,676,675 | A/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.