Human gene
POMT1 protein O-mannosyltransferase 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 |
|---|---|---|---|---|---|---|
| 3080 | Dystroglycanopathy, POMT1-related | Rhesus monkey | POMT1 | one to one | Target evidence |
57.8
|
Target evidence
Each Open Targets association between this gene and a human disease that a disease group reached.
| Human disease | Mondo | Score | Evidence |
|---|---|---|---|
| muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1 | MONDO:0009364 | 0.82 | 216 |
| muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 1 | MONDO:0013159 | 0.79 | 1,033 |
| muscular dystrophy-dystroglycanopathy | MONDO:0018276 | 0.01 | 5 |
Drugs
Each ChEMBL drug that acts on this gene.
No ChEMBL drug acts on this gene, among the genes with target evidence.