Comparative

Human gene

OPA3 optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)

ENSG00000125741 on Ensembl

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
162 Cardiomyopathy, dilated domestic cattle OPA3 one to one Drug 53.6
for Barth syndrome

Target evidence

Each Open Targets association between this gene and a human disease that a disease group reached.

Human disease Mondo Score Evidence
Barth syndrome MONDO:0010543 0.00 4

Drugs

Each ChEMBL drug that acts on this gene.

No ChEMBL drug acts on this gene, among the genes with target evidence.