Entity Details

Primary name COMP_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP49747
EntryNameCOMP_HUMAN
FullNameCartilage oligomeric matrix protein
TaxID9606
Evidenceevidence at protein level
Length757
SequenceStatuscomplete
DateCreated1996-10-01
DateModified2021-06-02

Ontological Relatives

GenesCOMP

GO terms

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GOName
GO:0001501 skeletal system development
GO:0002020 protease binding
GO:0002063 chondrocyte development
GO:0003417 growth plate cartilage development
GO:0005178 integrin binding
GO:0005201 extracellular matrix structural constituent
GO:0005509 calcium ion binding
GO:0005518 collagen binding
GO:0005576 extracellular region
GO:0005615 extracellular space
GO:0006915 apoptotic process
GO:0006986 response to unfolded protein
GO:0008201 heparin binding
GO:0009306 protein secretion
GO:0009887 animal organ morphogenesis
GO:0010259 multicellular organism aging
GO:0010260 animal organ senescence
GO:0010468 regulation of gene expression
GO:0014829 vascular associated smooth muscle contraction
GO:0016485 protein processing
GO:0030198 extracellular matrix organization
GO:0030199 collagen fibril organization
GO:0030282 bone mineralization
GO:0030500 regulation of bone mineralization
GO:0030509 BMP signaling pathway
GO:0031012 extracellular matrix
GO:0032991 protein-containing complex
GO:0035264 multicellular organism growth
GO:0035988 chondrocyte proliferation
GO:0035989 tendon development
GO:0036122 BMP binding
GO:0043066 negative regulation of apoptotic process
GO:0043394 proteoglycan binding
GO:0043395 heparan sulfate proteoglycan binding
GO:0043588 skin development
GO:0048844 artery morphogenesis
GO:0050881 musculoskeletal movement
GO:0050905 neuromuscular process
GO:0060173 limb development
GO:0062023 collagen-containing extracellular matrix
GO:0070062 extracellular exosome
GO:0070527 platelet aggregation
GO:0097084 vascular associated smooth muscle cell development
GO:1900047 negative regulation of hemostasis
GO:1902732 positive regulation of chondrocyte proliferation

Subcellular Location

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Subcellular Location
Secreted

Domains

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DomainNameCategoryType
IPR000742 EGF-like domainDomainDomain
IPR001881 EGF-like calcium-binding domainDomainDomain
IPR003367 Thrombospondin, type 3-like repeatRepeatRepeat
IPR008859 Thrombospondin, C-terminalDomainDomain
IPR009030 Growth factor receptor cysteine-rich domain superfamilyFamilyHomologous superfamily
IPR013320 Concanavalin A-like lectin/glucanase domain superfamilyFamilyHomologous superfamily
IPR017897 Thrombospondin, type 3 repeatRepeatRepeat
IPR018097 EGF-like calcium-binding, conserved siteSiteConserved site
IPR024665 Thrombospondin/cartilage oligomeric matrix protein, coiled-coil domainDomainDomain
IPR028492 Thrombospondin-5FamilyFamily
IPR028974 TSP type-3 repeatFamilyHomologous superfamily
IPR039081 Thrombospondin-5, coiled coil regionDomainDomain

Diseases

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Disease IDSourceNameDescription
132400 OMIMMultiple epiphyseal dysplasia 1 (EDM1)A generalized skeletal dysplasia associated with significant morbidity. Joint pain, joint deformity, waddling gait, and short stature are the main clinical signs and symptoms. Radiological examination of the skeleton shows delayed, irregular mineralization of the epiphyseal ossification centers and of the centers of the carpal and tarsal bones. Multiple epiphyseal dysplasia is broadly categorized into the more severe Fairbank and the milder Ribbing types. The Fairbank type is characterized by shortness of stature, short and stubby fingers, small epiphyses in several joints, including the knee, ankle, hand, and hip. The Ribbing type is confined predominantly to the hip joints and is characterized by hands that are normal and stature that is normal or near-normal. The disease is caused by variants affecting the gene represented in this entry.
177170 OMIMPseudoachondroplasia (PSACH)A skeletal dysplasia usually manifesting in the second year of life and characterized by moderate to severe disproportionate short stature, deformity of the lower limbs, brachydactyly, ligamentous laxity, and degenerative joint disease. The disease is caused by variants affecting the gene represented in this entry.

Drugs

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DrugNameSourceType
DB01373 CalciumDrugbanksmall molecule