Human gene
SPTBN4 spectrin, beta, non-erythrocytic 4
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 |
|---|---|---|---|---|---|---|
| 2232 | Myopathy, congenital, SPTBN4-related | pig | SPTBN4 | one to one | Target evidence |
56.2
|
Target evidence
Each Open Targets association between this gene and a human disease that a disease group reached.
| Human disease | Mondo | Score | Evidence |
|---|---|---|---|
| neurodevelopmental disorder with hypotonia, neuropathy, and deafness | MONDO:0060496 | 0.78 | 90 |
Drugs
Each ChEMBL drug that acts on this gene.
No ChEMBL drug acts on this gene, among the genes with target evidence.