Query author contributions in Reactome

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Details on Person SLC25A15 E180K [mitochondrial inner membrane]

Class:Id	EntityWithAccessionedSequence:9959772
_displayName	SLC25A15 E180K [mitochondrial inner membrane]
_timestamp	2025-07-01 19:22:31
compartment	[Compartment:70616] mitochondrial inner membrane
created	[InstanceEdit:9959767] Rothfels, Karen, 2025-07-01
crossReference	[DatabaseIdentifier:9959753] ClinGen:CA312984
disease	[Disease:9956498] ornithine translocase deficiency
endCoordinate	301
hasModifiedResidue	[ReplacedResidue:9959673] L-glutamic acid 180 replaced with L-lysine
literatureReference	[LiteratureReference:70619] Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter
name	SLC25A15 E180K 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:9959786] R-HSA-9959772.1
startCoordinate	1
(hasMember)	[CandidateSet:9956499] SLC25A15 variants [mitochondrial inner membrane] [Homo sapiens]
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No pathways have been reviewed or authored by SLC25A15 E180K [mitochondrial inner membrane] (9959772)