| AA | Ascorbic acid |
| ALR | Autophagic lysosome reformation |
| ATS | Arterial tortuosity syndrome |
| DHA | Dehydroascorbic acid |
| EST | Expressed sequence tag |
| ER | Endoplasmic reticulum |
| HIF | Hypoxia Inducible factor |
| HMIT | Human myoinositol transporter |
| G6P | Glucose-6-phosphate |
| G6PT | Glucose-6-phosphate transporter |
| G6Pase | Glucose-6-phosphatase |
| G6PC | Glucose-6-phosphatase |
| GLUT | Glucose transporter |
| GO | Gene ontology |
| GSD | Glycogen storage disease |
| GSD1rs | Glycogen storage disease 1 related syndrome |
| LPS | Lipopolysaccharide |
| mTOR | Mammalian target of rapamycin |
| Nf-kB | Nuclear factor kappa B |
| OST | Oligosaccharyl-transferase |
| Pi | Inorganic phosphate |
| ROS | Reactive oxygen species |
| SCN4 | Severe congenital neutropenia type 4 |
| SGLT | Sodium-glucose cotransporter |
| SLC | Solute carrier |
| SMIT2 | Sodium-myoinositol cotransporter 2 |
| SPNS | Spinster homologue |
| SVCT | Sodium couplet ascorbic acid transporter |
| SVM | Support vector machine |
| TET | Ten-eleven translocation |