Gene Ontology annotation through association of InterPro records with GO terms.

Annotation inferences using phylogenetic trees

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

Combined Automated Annotation using Multiple IEA Methods.

Cartilage oligomeric matrix protein is a calcium-binding protein, and a mutation in its type 3 repeats causes conformational changes.

Mutations in cartilage oligomeric matrix protein causing pseudoachondroplasia and multiple epiphyseal dysplasia affect binding of calcium and collagen I, II, and IX.

Matrix-matrix interaction of cartilage oligomeric matrix protein and fibronectin.

Interactions between the cartilage oligomeric matrix protein and matrilins. Implications for matrix assembly and the pathogenesis of chondrodysplasias.

Cartilage oligomeric matrix protein/thrombospondin 5 supports chondrocyte attachment through interaction with integrins.

Cartilage oligomeric matrix protein is involved in human limb development and in the pathogenesis of osteoarthritis.

ADAMTS-12 associates with and degrades cartilage oligomeric matrix protein.

Interaction of cartilage oligomeric matrix protein/thrombospondin 5 with aggrecan.

Cartilage oligomeric matrix protein protects cells against death by elevating members of the IAP family of survival proteins.

Extracellular matrix retention of thrombospondin 1 is controlled by its conserved C-terminal region.

Inhibition of ADAMTS-7 and ADAMTS-12 degradation of cartilage oligomeric matrix protein by alpha-2-macroglobulin.

Proteomics characterization of extracellular space components in the human aorta.

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

A proteome-scale map of the human interactome network.

Extracellular matrix remodelling in response to venous hypertension: proteomics of human varicose veins.

Lubricin binds cartilage proteins, cartilage oligomeric matrix protein, fibronectin and collagen II at the cartilage surface.

Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations.

A reference map of the human binary protein interactome.

Author Correction: Mutations in COMP cause familial carpal tunnel syndrome.

Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein gene.

Characterization of human and mouse cartilage oligomeric matrix protein.

COMP binds collagen, fibronectin, aggrecan and matrilins

COMP binds Integrin alpha5beta1, Integrin alphaVbeta3, CD47

Deep research on COMP function