Entity Details

Primary name ASPN_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9BXN1
EntryNameASPN_HUMAN
FullNameAsporin
TaxID9606
Evidenceevidence at protein level
Length380
SequenceStatuscomplete
DateCreated2002-06-20
DateModified2021-06-02

Ontological Relatives

GenesASPN

GO terms

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GOName
GO:0005509 calcium ion binding
GO:0005518 collagen binding
GO:0005615 extracellular space
GO:0030282 bone mineralization
GO:0030512 negative regulation of transforming growth factor beta receptor signaling pathway
GO:0031012 extracellular matrix
GO:0062023 collagen-containing extracellular matrix
GO:0070171 negative regulation of tooth mineralization

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
IPR028548 AsporinFamilyFamily
IPR032675 Leucine-rich repeat domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
603932 OMIMIntervertebral disc disease (IDD)A common musculo-skeletal disorder caused by degeneration of intervertebral disks of the lumbar spine. It results in low-back pain and unilateral leg pain. Disease susceptibility is associated with variants affecting the gene represented in this entry. Susceptibility to intervertebral disk disease, particularly lumbar disk degeneration, is conferred by a triplet repeat expansion polymorphism. ASPN allele having 14 aspartic acid repeats in the N-terminal region of the protein (D14), is associated with the disorder in some populations (PubMed:18304494).
607850 OMIMOsteoarthritis 3 (OS3)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. Disease susceptibility is associated with variants affecting the gene represented in this entry. Susceptibility to osteoarthritis is conferred by a triplet repeat expansion polymorphism. ASPN allele having 14 aspartic acid repeats in the N-terminal region of the protein (D14), is overrepresented relative to the common allele having 13 aspartic acid repeats (D13). The frequency of the D14 allele increases with disease severity. The D14 allele is also overrepresented in individuals with hip osteoarthritis.

Interactions

1 interaction

InteractorPartnerSourcesPublicationsLink
ASPN_HUMANPSMD2_HUMANBioGRID31136974 details