Gene Ontology annotation through association of InterPro records with GO terms

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

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

Electronic Gene Ontology annotations created by ARBA machine learning models

Combined Automated Annotation using Multiple IEA Methods

FERM protein EPB41L5 is a novel member of the mammalian CRB-MPP5 polarity complex.

Large-scale proteomics and phosphoproteomics of urinary exosomes.

Human CRB2 inhibits gamma-secretase cleavage of amyloid precursor protein by binding to the presenilin complex.

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

CRB2 completes a fully expressed Crumbs complex in the Retinal Pigment Epithelium.

Quantitative fragmentomics allow affinity mapping of interactomes.

Complete sequencing and characterization of 21,243 full-length human cDNAs.

Characterization of the Crumbs homolog 2 (CRB2) gene and analysis of its role in retinitis pigmentosa and Leber congenital amaurosis.

oko meduzy and related crumbs genes are determinants of apical cell features in the vertebrate embryo.

Pals1/Mpp5 is required for correct localization of Crb1 at the subapical region in polarized Muller glia cells.

Establishment of a neuroepithelial barrier by Claudin5a is essential for zebrafish brain ventricular lumen expansion.

The apical complex couples cell fate and cell survival to cerebral cortical development.

Dual roles of Notch in regulation of apically restricted mitosis and apicobasal polarity of neuroepithelial cells.

Deficiency in Crumbs homolog 2 (Crb2) affects gastrulation and results in embryonic lethality in mice.

Crb apical polarity proteins maintain zebrafish retinal cone mosaics via intercellular binding of their extracellular domains.

Loss of CRB2 in the mouse retina mimics human retinitis pigmentosa due to mutations in the CRB1 gene.

Spatial-temporal expressions of Crumbs and Nagie oko and their interdependence in zebrafish central nervous system during early development.

Defects of CRB2 cause steroid-resistant nephrotic syndrome.

Common and distinctive localization patterns of Crumbs polarity complex proteins in the mammalian eye.

Protein O-Glucosyltransferase 1 (POGLUT1) Promotes Mouse Gastrulation through Modification of the Apical Polarity Protein CRUMBS2.

Crumbs2 promotes cell ingression during the epithelial-to-mesenchymal transition at gastrulation.

Long-term clinicopathologic observation in a case of steroid-resistant nephrotic syndrome caused by a novel Crumbs homolog 2 mutation.

Key Role for CRB2 in the Maintenance of Apicobasal Polarity in Retinal Pigment Epithelial Cells.

Author Correction: Quantitative fragmentomics allow affinity mapping of interactomes.

Human CRB1 and CRB2 form homo- and heteromeric protein complexes in the retina.

CRB2 depletion induces YAP signaling and disrupts mechanosensing in podocytes.