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O15232 Proteins EGF-like domain Repeats
Uniprot ID:O15232
Protein name: Matrilin-3
Gene : MATN3
Protein Family:
Squence Length : 486
Sequnce
>O15232 487 MPRPAPARRLPGLLLLLWPLLLLPSAAPDPVARPGFRRLETRGPGGSPGRRPSPAAPDGAPASGTSEPGRARGAGVCKSRPLDLVFIIDSSRSVRPLEFTKVKTFVSRIIDTLDIGPADTRVAVVNYASTVKIEFQLQAYTDKQSLKQAVGRITPLSTGTMSGLAIQTAMDEAFTVEAGAREPSSNIPKVAIIVTDGRPQDQVNEVAARAQASGIELYAVGVDRADMASLKMMASEPLEEHVFYVETYGVIEKLSSRFQETFCALDPCVLGTHQCQHVCISDGEGKHHCECSQGYTLNADKKTCSALDRCALNTHGCEHICVNDRSGSYHCECYEGYTLNEDRKTCSAQDKCALGTHGCQHICVNDRTGSHHCECYEGYTLNADKKTCSVRDKCALGSHGCQHICVSDGAASYHCDCYPGYTLNEDKKTCSATEEARRLVSTEDACGCEATLAFQDKVSSYLQRLNTKLDDILEKLKINEYGQIHR
Domains
DOMAIN 83 258 VWFA DOMAIN 264 305 EGF-like 1 DOMAIN 306 347 EGF-like 2 DOMAIN 348 389 EGF-like 3 DOMAIN 390 431 EGF-like 4
EGF-like sequence regions
264 - 305 DPCVLGTHQCQHVCISDGEGKHHCECSQGYTLNADKKTCSAL 306 - 347 DRCALNTHGCEHICVNDRSGSYHCECYEGYTLNEDRKTCSAQ 348 - 389 DKCALGTHGCQHICVNDRTGSHHCECYEGYTLNADKKTCSVR 390 - 431 DKCALGSHGCQHICVSDGAASYHCDCYPGYTLNEDKKTCSAT
Function
Major component of the extracellular matrix of cartilage and may play a role in the formation of extracellular filamentous networks
Disease
"DISEASE: Multiple epiphyseal dysplasia 5 (EDM5) [MIM:607078]: 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 Note=The disease is caused by mutations affecting the gene represented in this entry ; DISEASE: Spondyloepimetaphyseal dysplasia MATN3-related (SEMD-MATN3) [MIM:608728]: 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 Note=The disease is caused by mutations affecting the gene represented in this entry ; DISEASE: Osteoarthritis 2 (OS2) [MIM:140600]: 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 Note=Disease susceptibility is associated with variations affecting the gene represented in this entry"