Entity Details

Primary name MGP_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP08493
EntryNameMGP_HUMAN
FullNameMatrix Gla protein
TaxID9606
Evidenceevidence at protein level
Length103
SequenceStatuscomplete
DateCreated1988-08-01
DateModified2021-06-02

Ontological Relatives

GenesMGP

GO terms

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GOName
GO:0001502 cartilage condensation
GO:0001503 ossification
GO:0005201 extracellular matrix structural constituent
GO:0005509 calcium ion binding
GO:0008147 structural constituent of bone
GO:0030154 cell differentiation
GO:0030500 regulation of bone mineralization
GO:0031012 extracellular matrix
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
IPR000294 Gamma-carboxyglutamic acid-rich (GLA) domainDomainDomain
IPR002384 Osteocalcin/matrix Gla proteinFamilyFamily
IPR027118 Matrix Gla proteinFamilyFamily
IPR035972 Gamma-carboxyglutamic acid-rich (GLA) domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
245150 OMIMKeutel syndrome (KTLS)An autosomal recessive disorder characterized by abnormal cartilage calcification, peripheral pulmonary stenosis neural hearing loss and midfacial hypoplasia. The disease is caused by variants affecting the gene represented in this entry.

Drugs

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DrugNameSourceType
DB01373 CalciumDrugbanksmall molecule

Interactions

2 interactions

InteractorPartnerSourcesPublicationsLink
MGP_HUMANBMP2_HUMANBioGRID, HPRD11741887 details
MGP_HUMANHIS3_HUMANBioGRID26544073 details