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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 MECP2_e2 P302R [nucleoplasm]

Class:IdEntityWithAccessionedSequence:9005588
_displayNameMECP2_e2 P302R [nucleoplasm]
_timestamp2017-05-09 13:47:36
compartment[Compartment:7660] nucleoplasm
created[InstanceEdit:9005571] Orlic-Milacic, Marija, 2017-05-09
disease[Disease:9005548] Rett syndrome
endCoordinate486
hasModifiedResidue[ReplacedResidue:9005544] L-proline 302 replaced with L-arginine
literatureReference[LiteratureReference:9005560] A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome
[LiteratureReference:9005556] Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor
nameMECP2_e2 P302R
MECP2A P302R
referenceEntity[ReferenceIsoform:404286] UniProt:P51608-1 MECP2 [Homo sapiens]
species[Species:48887] Homo sapiens
stableIdentifier[StableIdentifier:9005610] R-HSA-9005588.1
startCoordinate1
(hasMember)[CandidateSet:9005538] MECP2 P304R [nucleoplasm] [Homo sapiens]
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No pathways have been reviewed or authored by MECP2_e2 P302R [nucleoplasm] (9005588)