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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 SLC25A15 [mitochondrial inner membrane]

Class:IdEntityWithAccessionedSequence:70618
_displayNameSLC25A15 [mitochondrial inner membrane]
_timestamp2008-07-24 20:44:56
compartment[Compartment:70616] mitochondrial inner membrane
endCoordinate301
literatureReference[LiteratureReference:70619] Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter
[Book:70631] The hyperornithinemias 0079130356 Scriver, Charles R The Metabolic and Molecular Bases of Inherited Disease, 8th ed
modified[InstanceEdit:113604] Schmidt, EE, 2004-06-09 05:34:08
[InstanceEdit:374021] D'Eustachio, P, 2008-07-24 20:44:45
[InstanceEdit:3132750] Wu, G, 2013-02-13
nameSLC25A15
Mitochondrial ornithine transporter 1
Solute carrier family 25, member 15
referenceEntity[ReferenceGeneProduct:61004] UniProt:Q9Y619 SLC25A15 [Homo sapiens]
species[Species:48887] Homo sapiens
stableIdentifier[StableIdentifier:370412] R-HSA-70618.1
startCoordinate1
(hasMember)[DefinedSet:374018] Mitochondrial ornithine transporters [mitochondrial inner membrane] [Homo sapiens]
(updatedInstance)[_UpdateTracker:9867827] Update Tracker - [EntityWithAccessionedSequence:70618] SLC25A15 [mitochondrial inner membrane] - v26:[addName]
[_UpdateTracker:9874663] Update Tracker - [EntityWithAccessionedSequence:70618] SLC25A15 [mitochondrial inner membrane] - v44:[modifyEndCoordinate]
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No pathways have been reviewed or authored by SLC25A15 [mitochondrial inner membrane] (70618)
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