Comparative

Human gene

SGCA sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein)

ENSG00000108823 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
2305 Muscular dystrophy, limb-girdle, type R3 (LGMDR3) dog SGCA one to one Target evidence 63.2
for autosomal recessive limb-girdle muscular dystrophy type 2D

Target evidence

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

Human disease Mondo Score Evidence
autosomal recessive limb-girdle muscular dystrophy type 2D MONDO:0011968 0.84 814

Drugs

Each ChEMBL drug that acts on this gene.

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