Human gene
SPTBN2 spectrin, beta, non-erythrocytic 2
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 |
|---|---|---|---|---|---|---|
| 2092 | Ataxia, spinocerebellar, SPTBN2-related | dog | SPTBN2 | one to one | Target evidence |
57.0
|
Target evidence
Each Open Targets association between this gene and a human disease that a disease group reached.
| Human disease | Mondo | Score | Evidence |
|---|---|---|---|
| spinocerebellar ataxia type 5 | MONDO:0010848 | 0.80 | 173 |
| autosomal recessive spinocerebellar ataxia 14 | MONDO:0014159 | 0.77 | 91 |
Drugs
Each ChEMBL drug that acts on this gene.
No ChEMBL drug acts on this gene, among the genes with target evidence.