Annotation inferences using phylogenetic trees

Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt

Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara

Electronic Gene Ontology annotations created by ARBA machine learning models

Mutation screening of USH3 gene (clarin-1) in Spanish patients with Usher syndrome: low prevalence and phenotypic variability.

Serial audiometry and speech recognition findings in Finnish Usher syndrome type III patients.

Clarin-1, encoded by the Usher Syndrome III causative gene, forms a membranous microdomain: possible role of clarin-1 in organizing the actin cytoskeleton.

CLRN1 mutations cause nonsyndromic retinitis pigmentosa.

Clarin-1 gene transfer rescues auditory synaptopathy in model of Usher syndrome.

A reference map of the human binary protein interactome.

Deep research on CLRN1 function