Entity Details

Primary name PGS1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP21810
EntryNamePGS1_HUMAN
FullNameBiglycan
TaxID9606
Evidenceevidence at protein level
Length368
SequenceStatuscomplete
DateCreated1991-05-01
DateModified2021-06-02

Ontological Relatives

GenesBGN

GO terms

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GOName
GO:0001974 blood vessel remodeling
GO:0005201 extracellular matrix structural constituent
GO:0005539 glycosaminoglycan binding
GO:0005576 extracellular region
GO:0005615 extracellular space
GO:0005796 Golgi lumen
GO:0009986 cell surface
GO:0019800 peptide cross-linking via chondroitin 4-sulfate glycosaminoglycan
GO:0030021 extracellular matrix structural constituent conferring compression resistance
GO:0030133 transport vesicle
GO:0030198 extracellular matrix organization
GO:0030206 chondroitin sulfate biosynthetic process
GO:0030207 chondroitin sulfate catabolic process
GO:0030208 dermatan sulfate biosynthetic process
GO:0031012 extracellular matrix
GO:0042383 sarcolemma
GO:0043202 lysosomal lumen
GO:0050840 extracellular matrix binding
GO:0060348 bone development
GO:0061975 articular cartilage development
GO:0062023 collagen-containing extracellular matrix
GO:0070062 extracellular exosome

Subcellular Location

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Subcellular Location
Secreted

Domains

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DomainNameCategoryType
IPR000372 Leucine-rich repeat N-terminal domainDomainDomain
IPR001611 Leucine-rich repeatRepeatRepeat
IPR003591 Leucine-rich repeat, typical subtypeRepeatRepeat
IPR016352 Small leucine-rich proteoglycan, class I, decorin/asporin/byglycanFamilyFamily
IPR028547 BiglycanFamilyFamily
IPR032675 Leucine-rich repeat domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
300989 OMIMMeester-Loeys syndrome (MRLS)An X-linked, thoracic aortic aneurysm syndrome characterized by early-onset, severe aortic aneurysm and dissection. Other recurrent findings include hypertelorism, pectus deformity, joint hypermobility, contractures, and mild skeletal dysplasia. The disease is caused by variants affecting the gene represented in this entry.
300106 OMIMSpondyloepimetaphyseal dysplasia, X-linked (SEMDX)An X-linked recessive bone disease characterized by severe short-trunk dwarfism, brachydactyly, metaphyseal flaring of lower extremities, short and broad long bone diaphyses, moderate platyspondyly, normal facies, and normal intelligence. The disease is caused by variants affecting the gene represented in this entry.