GLTPD2
glycolipid transfer protein domain containing 2
Summary
Predicted to enable ceramide 1-phosphate binding activity and ceramide 1-phosphate transfer activity. Predicted to be involved in ceramide transport and intermembrane lipid transfer. Predicted to be located in cytoplasm. Predicted to be active in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs190261815 | 17:4,692,154 | C/T | regulatory region variant | — |
| rs200715683 | 17:4,692,323 | G/A | — | uncertain significance |
| rs2150654450 | 17:4,692,379 | C/G | — | uncertain significance |
| rs373630469 | 17:4,692,548 | C/T | — | uncertain significance |
| rs202226463 | 17:4,692,568 | G/C | — | uncertain significance |
| rs79202680 | 17:4,692,640 | G/T | regulatory region variant | — |
| rs954565904 | 17:4,692,876 | T/G | — | uncertain significance |
| rs375244706 | 17:4,692,877 | G/A | — | uncertain significance |
| rs1567712319 | 17:4,693,083 | C/T | — | uncertain significance |
| rs374100494 | 17:4,693,126 | G/T | — | uncertain significance |
| rs973259137 | 17:4,693,194 | G/A | — | uncertain significance |
| rs373390253 | 17:4,693,221 | C/T | — | uncertain significance |
| rs750635969 | 17:4,693,224 | C/T | — | uncertain significance |
| rs199986886 | 17:4,693,253 | T/C | — | uncertain significance |
| rs1917625241 | 17:4,693,256 | C/T | — | uncertain significance |
| rs1567712496 | 17:4,693,275 | A/G | — | uncertain significance |
| rs971374901 | 17:4,693,310 | C/G | — | uncertain significance |
| rs1917626777 | 17:4,693,313 | G/A | — | uncertain significance |
| rs35910358 | 17:4,693,342 | C/A | missense variant | — |
| rs1354110702 | 17:4,693,357 | C/G | — | uncertain significance |
| rs973091317 | 17:4,693,367 | T/A | — | uncertain significance |
| rs1184165883 | 17:4,693,374 | C/A | — | uncertain significance |
| rs1316615097 | 17:4,693,383 | G/C | — | likely benign |
| rs369571991 | 17:4,693,445 | C/T | — | uncertain significance |
| rs1375502403 | 17:4,693,484 | G/C | — | likely benign |
| rs536055318 | 17:4,693,502 | G/A | missense variant | — |
| rs765238837 | 17:4,693,566 | A/G | — | uncertain significance |
| rs1350396870 | 17:4,693,568 | C/G | — | uncertain significance |
| rs73339979 | 17:4,693,902 | G/C | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.