Query author contributions in Reactome

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Details on Person SHOC2 S2G [cytosol]

Class:Id	EntityWithAccessionedSequence:9660457
_displayName	SHOC2 S2G [cytosol]
_timestamp	2019-09-09 19:51:09
compartment	[Compartment:70101] cytosol
created	[InstanceEdit:9660460] Rothfels, Karen, 2019-09-09
crossReference	[DatabaseIdentifier:9660458] ClinGen:CA118524 [DatabaseIdentifier:9660459] COSMIC:COSV54624833
disease	[Disease:6802289] Noonan syndrome [Disease:1247687] chronic myeloid leukemia
endCoordinate	582
hasModifiedResidue	[ReplacedResidue:9660461] L-serine 2 replaced with glycine
literatureReference	[LiteratureReference:9660412] Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair
name	SHOC2 S2G Leucine-rich repeat protein SHOC-2 SHOC2_HUMAN
referenceEntity	[ReferenceGeneProduct:64440] UniProt:Q9UQ13 SHOC2 [Homo sapiens]
species	[Species:48887] Homo sapiens
stableIdentifier	[StableIdentifier:9660462] R-HSA-9660457.1
startCoordinate	1
(hasMember)	[DefinedSet:9660468] SHOC2 gain-of-function mutants [cytosol] [Homo sapiens]
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No pathways have been reviewed or authored by SHOC2 S2G [cytosol] (9660457)