Human gene
SLC2A2 solute carrier family 2 (facilitated glucose transporter), member 2
2 disease groups in OMIA reach this gene, through the animal gene that Ensembl gives as its ortholog. The page shows the chain. It does not say whether an animal is a model of a human disease.
Animal diseases
By each group's best natural-model score, highest first. How the score works.
| OMIA group | Name | Species | Animal gene | Ortholog | The chain reached | Best score |
|---|---|---|---|---|---|---|
| 366 | Fanconi syndrome | domestic cattle | SLC2A2 | one to one | Target evidence |
63.7
|
| 1958 | Growth retardation due to haplotype FH2 | domestic cattle | SLC2A2 | one to one | Animal disease only |
Target evidence
Each Open Targets association between this gene and a human disease that a disease group reached.
| Human disease | Mondo | Score | Evidence |
|---|---|---|---|
| glycogen storage disease due to GLUT2 deficiency | MONDO:0009216 | 0.82 | 442 |
Drugs
Each ChEMBL drug that acts on this gene.
No ChEMBL drug acts on this gene, among the genes with target evidence.