Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1311
Gene Symbol: COMP
COMP
0.060 Biomarker disease BEFREE Genotype to phenotype correlations in cartilage oligomeric matrix protein associated chondrodysplasias. 24595329 2014
Entrez Id: 1311
Gene Symbol: COMP
COMP
0.060 Biomarker disease BEFREE This constitutes a novel pathogenetic mechanism of COMP-associated chondrodysplasias. 20936634 2011
Entrez Id: 1311
Gene Symbol: COMP
COMP
0.060 GeneticVariation disease BEFREE Mutations in matrilin-3 have been associated with common skeletal diseases like osteoarthritis as well as with the rare chondrodysplasias MED and SEMD. 20077500 2010
Entrez Id: 1311
Gene Symbol: COMP
COMP
0.060 GeneticVariation disease BEFREE Pseudoachondroplasia (PSACH) is a dominantly inherited chondrodysplasia associated with mutations of cartilage oligomeric matrix protein (COMP), characterized clinically by disproportionate dwarfism and laxity of joints and ligaments. 17307347 2007
Entrez Id: 1311
Gene Symbol: COMP
COMP
0.060 GeneticVariation disease BEFREE These observations are similar to those for mutations in the cartilage oligomeric matrix protein (COMP) leading to multiple epiphyseal dysplasia and pseudoachondroplasia suggesting that retention and accumulation of cartilage proteins in the ER might be a general mechanism involved in the pathogenesis of chondrodysplasias. 16199550 2005
Entrez Id: 1311
Gene Symbol: COMP
COMP
0.060 GeneticVariation disease BEFREE Mutations in the cartilage oligomeric matrix protein (COMP) gene result in pseudoachondroplasia (PSACH), which is a chondrodysplasia characterized by early-onset osteoarthritis and short stature. 11691584 2001