Entity Details

Primary name MATN3_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionO15232
EntryNameMATN3_HUMAN
FullNameMatrilin-3
TaxID9606
Evidenceevidence at protein level
Length486
SequenceStatuscomplete
DateCreated2001-06-20
DateModified2021-06-02

Ontological Relatives

GenesMATN3

GO terms

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GOName
GO:0001501 skeletal system development
GO:0005201 extracellular matrix structural constituent
GO:0005509 calcium ion binding
GO:0005576 extracellular region
GO:0005788 endoplasmic reticulum lumen
GO:0030198 extracellular matrix organization
GO:0031012 extracellular matrix
GO:0043687 post-translational protein modification
GO:0044267 cellular protein metabolic process
GO:0051216 cartilage development
GO:0062023 collagen-containing extracellular matrix

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
IPR002035 von Willebrand factor, type ADomainDomain
IPR009030 Growth factor receptor cysteine-rich domain superfamilyFamilyHomologous superfamily
IPR019466 Matrilin, coiled-coil trimerisation domainDomainDomain
IPR030765 Matrilin 3FamilyFamily
IPR036337 Matrilin, coiled-coil domain superfamilyFamilyHomologous superfamily
IPR036465 von Willebrand factor A-like domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
608728 OMIMSpondyloepimetaphyseal dysplasia, MATN3-related (SEMD-MATN3)A bone disease characterized by disproportionate early-onset dwarfism, bowing of the lower limbs, lumbar lordosis and normal hands. Skeletal abnormalities include short, wide and stocky long bones with severe epiphyseal and metaphyseal changes, hypoplastic iliac bones and flat, ovoid vertebral bodies. The disease is caused by variants affecting the gene represented in this entry.
607078 OMIMMultiple epiphyseal dysplasia 5 (EDM5)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. Multiple epiphyseal dysplasia type 5 is relatively mild and clinically variable. It is primarily characterized by delayed and irregular ossification of the epiphyses and early-onset osteoarthritis. The disease is caused by variants affecting the gene represented in this entry.
140600 OMIMOsteoarthritis 2 (OS2)A degenerative disease of the joints characterized by degradation of the hyaline articular cartilage and remodeling of the subchondral bone with sclerosis. Clinical symptoms include pain and joint stiffness often leading to significant disability and joint replacement. In the hand, osteoarthritis can develop in the distal interphalangeal and the first carpometacarpal (base of thumb) and proximal interphalangeal joints. Patients with osteoarthritis may have one, a few, or all of these sites affected. Disease susceptibility is associated with variants affecting the gene represented in this entry.