Entity Details

Primary name CO6A3_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP12111
EntryNameCO6A3_HUMAN
FullNameCollagen alpha-3(VI) chain
TaxID9606
Evidenceevidence at protein level
Length3177
SequenceStatuscomplete
DateCreated1989-10-01
DateModified2021-06-02

Ontological Relatives

GenesCOL6A3

GO terms

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GOName
GO:0004867 serine-type endopeptidase inhibitor activity
GO:0005576 extracellular region
GO:0005589 collagen type VI trimer
GO:0005615 extracellular space
GO:0005788 endoplasmic reticulum lumen
GO:0007155 cell adhesion
GO:0007517 muscle organ development
GO:0030020 extracellular matrix structural constituent conferring tensile strength
GO:0030198 extracellular matrix organization
GO:0030199 collagen fibril organization
GO:0031012 extracellular matrix
GO:0042383 sarcolemma
GO:0062023 collagen-containing extracellular matrix
GO:0070062 extracellular exosome
GO:1903561 extracellular vesicle

Subcellular Location

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Subcellular Location
Secreted

Domains

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DomainNameCategoryType
IPR002035 von Willebrand factor, type ADomainDomain
IPR002223 Pancreatic trypsin inhibitor Kunitz domainDomainDomain
IPR003961 Fibronectin type IIIDomainDomain
IPR008160 Collagen triple helix repeatRepeatRepeat
IPR013783 Immunoglobulin-like foldFamilyHomologous superfamily
IPR020901 Proteinase inhibitor I2, Kunitz, conserved siteSiteConserved site
IPR036116 Fibronectin type III superfamilyFamilyHomologous superfamily
IPR036465 von Willebrand factor A-like domain superfamilyFamilyHomologous superfamily
IPR036880 Pancreatic trypsin inhibitor Kunitz domain superfamilyFamilyHomologous superfamily
IPR041900 Collagen alpha-3(VI) chain, vWA domainDomainDomain

Diseases

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Disease IDSourceNameDescription
158810 OMIMBethlem myopathy 1 (BTHLM1)A benign proximal myopathy characterized by early childhood onset and joint contractures most frequently affecting the elbows and ankles. The disease is caused by variants affecting the gene represented in this entry.
254090 OMIMUllrich congenital muscular dystrophy 1 (UCMD1)A congenital myopathy characterized by muscle weakness and multiple joint contractures, generally noted at birth or early infancy. The clinical course is more severe than in Bethlem myopathy. The disease is caused by variants affecting the gene represented in this entry.
616411 OMIMDystonia 27 (DYT27)A form of dystonia, a disorder defined by the presence of sustained involuntary muscle contraction, often leading to abnormal postures. DYT27 is an autosomal recessive form characterized by segmental isolated dystonia involving the face, neck, bulbar muscles, and upper limbs. The disease is caused by variants affecting the gene represented in this entry.