osteoarthritis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An arthritis that has_material_basis_in worn out cartilage located_in joint. (Human Disease Ontology, DOID_8398)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003560
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16 gene mutations causing the osteoarthritis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP7A ATPase, Cu++ transporting, alpha polypeptide
BGN biglycan
COL11A1 collagen, type XI, alpha 1
COL9A1 collagen, type IX, alpha 1
COMP cartilage oligomeric matrix protein
ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 1
ERRFI1 ERBB receptor feedback inhibitor 1
FMOD fibromodulin
HSPG2 heparan sulfate proteoglycan 2
HYAL1 hyaluronoglucosaminidase 1
LTBP3 latent transforming growth factor beta binding protein 3
MATN3 matrilin 3
MIR140 microRNA 140
MMP3 matrix metallopeptidase 3
PLCG2 phospholipase C, gamma 2 (phosphatidylinositol-specific)
SMAD3 SMAD family member 3