Comparative

Human gene

SLC35A3 solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member A3

ENSG00000117620 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
1340 Complex vertebral malformation domestic cattle SLC35A3 one to one Target evidence 62.1
for autism spectrum disorder - epilepsy - arthrogryposis syndrome

Target evidence

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

Human disease Mondo Score Evidence
autism spectrum disorder - epilepsy - arthrogryposis syndrome MONDO:0014248 0.77 303

Drugs

Each ChEMBL drug that acts on this gene.

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