Human gene
SLC33A1 solute carrier family 33 member 1
1 disease group in OMIA reaches 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 |
|---|---|---|---|---|---|---|
| 2862 | Haplotype with homozygous deficiency, SLC33A1-related | sheep | SLC33A1 | one to one | Target evidence |
54.3
|
Target evidence
Each Open Targets association between this gene and a human disease that a disease group reached.
| Human disease | Mondo | Score | Evidence |
|---|---|---|---|
| Huppke-Brendel syndrome | MONDO:0013772 | 0.72 | 24 |
| hereditary spastic paraplegia 42 | MONDO:0012928 | 0.63 | 19 |
Drugs
Each ChEMBL drug that acts on this gene.
No ChEMBL drug acts on this gene, among the genes with target evidence.