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Details on Person Defective collagen type X network [extracellular region]

Class:Id	Polymer:9017603
_displayName	Defective collagen type X network [extracellular region]
_timestamp	2017-08-23 11:53:48
compartment	[Compartment:984] extracellular region
created	[InstanceEdit:9017635] Varusai, Thawfeek, 2017-08-23
disease	[Disease:9017625] Schmid metaphyseal chondrodysplasia
literatureReference	[LiteratureReference:9017608] Insight into Schmid metaphyseal chondrodysplasia from the crystal structure of the collagen X NC1 domain trimer [LiteratureReference:9017618] Metaphyseal chondrodysplasia type Schmid mutations are predicted to occur in two distinct three-dimensional clusters within type X collagen NC1 domains that retain the ability to trimerize
modified	[InstanceEdit:9017680] Varusai, Thawfeek, 2017-08-23
name	Defective collagen type X network
repeatedUnit	[Complex:9017628] Defective tropocollagen type X [extracellular region] [Homo sapiens]
species	[Species:48887] Homo sapiens
stableIdentifier	[StableIdentifier:9017654] R-HSA-9017603.1
(hasComponent)	[Complex:9017720] Defective collagen type X:type II fibrils [extracellular region] [Homo sapiens] [Complex:9018705] COL10A1-defective collagen type X network:Integrin alpha2beta1 [plasma membrane] [Homo sapiens]
(hasMember)	[DefinedSet:9017612] COL10A1 defective collagen networks [extracellular region] [Homo sapiens]
(input)	[Reaction:9017722] Defective type X collagen associates with collagen type II fibrils [Homo sapiens] [Reaction:9018706] COL10A1-defective collagen type X binds Integrin alpha2beta1 [Homo sapiens]
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No pathways have been reviewed or authored by Defective collagen type X network [extracellular region] (9017603)