Entity Details

Primary name COL6A3
Entity type gene
Source Source Link

Details

PrimaryID1293
RefseqGeneNG_008676
SymbolCOL6A3
Namecollagen type VI alpha 3 chain
Chromosome2
Location2q37.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1998-08-27
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsCO6A3_HUMAN

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

Diseases

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Disease IDSourceNameDescription
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.
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.
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.

Interactions

10 interactions