Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity

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

Gene Ontology annotation based on curation of immunofluorescence data

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

Electronic Gene Ontology annotations created by ARBA machine learning models

The eps8 family of proteins links growth factor stimulation to actin reorganization generating functional redundancy in the Ras/Rac pathway.

Large-scale proteomics and phosphoproteomics of urinary exosomes.

Characterization of exosome-like vesicles released from human tracheobronchial ciliated epithelium: a possible role in innate defense.

Proteomic analysis of human parotid gland exosomes by multidimensional protein identification technology (MudPIT).

In-depth proteomic analyses of exosomes isolated from expressed prostatic secretions in urine.

E-cadherin interactome complexity and robustness resolved by quantitative proteomics.

Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains.

Progressive hearing loss and gradual deterioration of sensory hair bundles in the ears of mice lacking the actin-binding protein Eps8L2.

EPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing loss.

Molecular Analysis of Twelve Pakistani Families with Nonsyndromic or Syndromic Hearing Loss.

Ctdnep1 and Eps8L2 regulate dorsal actin cables for nuclear positioning during cell migration.

BAIAP2L2 is required for the maintenance of mechanotransducing stereocilia of cochlear hair cells.

Early onset adult deafness in the Rhodesian Ridgeback dog is associated with an in-frame deletion in the EPS8L2 gene.

Expansion of Molecular and Clinical Aspects of EPS8L2 (DFNB106)-Associated Hearing Loss Emphasizes a Potential Therapeutic Window.

UniProt entry Q9H6S3 (EPS8L2_HUMAN)

PANTHER PTHR12287 family member entries