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Details on Person DDR1 binds COL5A1-defective collagen type I, II, III, IV, V, XI fibrils

Class:IdReaction:9018064
_displayNameDDR1 binds COL5A1-defective collagen type I, II, III, IV, V, XI fibrils
_timestamp2017-08-29 09:44:35
compartment[Compartment:876] plasma membrane
[Compartment:984] extracellular region
created[InstanceEdit:9018065] Varusai, Thawfeek, 2017-08-29
disease[Disease:3656228] Ehlers-Danlos syndrome
input[Complex:2327930] DDR1 dimer [plasma membrane] [Homo sapiens]
[CandidateSet:9018066] COL5A1-defective collagen type I, II, III, IV, V, XI fibrils [extracellular region] [Homo sapiens]
isChimericFALSE
literatureReference[LiteratureReference:2327700] An orphan receptor tyrosine kinase family whose members serve as nonintegrin collagen receptors
[LiteratureReference:2465894] The discoidin domain receptor tyrosine kinases are activated by collagen
[LiteratureReference:9014027] Comprehensive molecular analysis demonstrates type V collagen mutations in over 90% of patients with classic EDS and allows to refine diagnostic criteria
[LiteratureReference:9014031] Order of intron removal influences multiple splice outcomes, including a two-exon skip, in a COL5A1 acceptor-site mutation that results in abnormal pro-alpha1(V) N-propeptides and Ehlers-Danlos syndrome type I
modified[InstanceEdit:9018082] Varusai, Thawfeek, 2017-08-29
nameDDR1 binds COL5A1-defective collagen type I, II, III, IV, V, XI fibrils
normalReaction
output[Complex:9018070] DDR1 dimer:COL5A1-defective collagen type I, II, III, IV, V, XI fibrils [plasma membrane] [Homo sapiens]
precedingEvent
species[Species:48887] Homo sapiens
stableIdentifier[StableIdentifier:9018081] R-HSA-9018064.1
summation[Summation:9018074] Discoidin domain receptors (DDRs) are a subfamily of recepto...
(hasEvent)[Pathway:9018067] Abnormal non-integrin membrane-ECM interactions [Homo sapiens]
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No pathways have been reviewed or authored by DDR1 binds COL5A1-defective collagen type I, II, III, IV, V, XI fibrils (9018064)