Reactome: A Curated Pathway Database
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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.

If you have an ORCID ID that is not listed on this page, please forward this information to us and we will update your Reactome pathway records.

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Details on Person COL10A1 S671P [extracellular region]

Class:IdEntityWithAccessionedSequence:9017674
_displayNameCOL10A1 S671P [extracellular region]
_timestamp2017-08-23 11:54:46
compartment[Compartment:984] extracellular region
created[InstanceEdit:9017680] Varusai, Thawfeek, 2017-08-23
disease[Disease:9017625] Schmid metaphyseal chondrodysplasia
endCoordinate680
hasModifiedResidue[ReplacedResidue:9017672] L-serine 671 replaced with L-aspartic acid
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
nameCOL10A1 S671P
referenceEntity[ReferenceGeneProduct:51144] UniProt:Q03692 COL10A1 [Homo sapiens]
species[Species:48887] Homo sapiens
stableIdentifier[StableIdentifier:9017686] R-HSA-9017674.1
startCoordinate1
(hasMember)[DefinedSet:9017673] COL10A1 class II mutants [extracellular region] [Homo sapiens]
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No pathways have been reviewed or authored by COL10A1 S671P [extracellular region] (9017674)