Entity Details

Primary name MGP
Entity type gene
Source Source Link

Details

PrimaryID4256
RefseqGeneNG_023331
SymbolMGP
Namematrix Gla protein
Chromosome12
Location12p12.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1991-10-30
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsMGP_HUMAN

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

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.

Interactions

2 interactions

InteractorPartnerSourcesPublicationsLink
MGPBMP2BioGRID, HPRD11741887 details
MGPHTN3BioGRID26544073 details