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Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

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Details on Person COL5A1 mutants [endoplasmic reticulum lumen]

Class:IdDefinedSet:9013596
_displayNameCOL5A1 mutants [endoplasmic reticulum lumen]
_timestamp2017-09-05 13:57:47
compartment[Compartment:17957] endoplasmic reticulum lumen
created[InstanceEdit:9013591] Varusai, Thawfeek, 2017-07-25
disease[Disease:3656228] Ehlers-Danlos syndrome
hasMember
literatureReference[LiteratureReference:9014027] Comprehensive molecular analysis demonstrates type V collagen mutations in over 90% of patients with classic EDS and allows to refine diagnostic criteria
modified[InstanceEdit:9013624] Varusai, Thawfeek, 2017-07-25
[InstanceEdit:9014026] Varusai, Thawfeek, 2017-07-26
[InstanceEdit:9019609] Varusai, Thawfeek, 2017-09-05
nameCOL5A1 mutants
species[Species:48887] Homo sapiens
stableIdentifier[StableIdentifier:9013617] R-HSA-9013596.1
(hasComponent)[Complex:9013585] Defective C-linked procollagen alpha-1-3(V) propeptide trimer [endoplasmic reticulum lumen] [Homo sapiens]
[Complex:9013606] Defective C-linked procollagen alpha-1(V)X2 alpha-2(V) trimer [endoplasmic reticulum lumen] [Homo sapiens]
(input)[Reaction:9013588] Defective procollagen type V [Homo sapiens]
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No pathways have been reviewed or authored by COL5A1 mutants [endoplasmic reticulum lumen] (9013596)