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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 R106W, MECP2 D121G,MECP2 R133H,MECP2S134F,MECP2 T158M/A [nucleoplasm]

Class:IdDefinedSet:9022525
_displayNameMECP2 R106W, MECP2 D121G,MECP2 R133H,MECP2S134F,MECP2 T158M/A [nucleoplasm]
_timestamp2017-09-27 15:38:31
compartment[Compartment:7660] nucleoplasm
created[InstanceEdit:9022524] Orlic-Milacic, Marija, 2017-09-25
disease[Disease:9005548] Rett syndrome
hasMember
modified[InstanceEdit:9023426] Orlic-Milacic, Marija, 2017-09-27
[InstanceEdit:9023448] Orlic-Milacic, Marija, 2017-09-27
[InstanceEdit:9023458] Orlic-Milacic, Marija, 2017-09-27
nameMECP2 R106W, MECP2 D121G,MECP2 R133H,MECP2S134F,MECP2 T158M/A
species[Species:48887] Homo sapiens
stableIdentifier[StableIdentifier:9022528] R-HSA-9022525.1
(diseaseEntity)[EntityFunctionalStatus:9022526] loss_of_function of MECP2 R106W, MECP2 D121G,MECP2 R133H,MECP2S134F,MECP2 T158M/A [nucleoplasm]
(hasMember)[DefinedSet:9022522] MECP2 R133C,MECP2 D121G,MECP2 R133H,MECP2 S134F [nucleoplasm] [Homo sapiens]
(input)[FailedReaction:9022465] MECP2 mutants R106W, D121G, R133H, S134F, T158M and T158A do not bind to 5mC-DNA [Homo sapiens]
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No pathways have been reviewed or authored by MECP2 R106W, MECP2 D121G,MECP2 R133H,MECP2S134F,MECP2 T158M/A [nucleoplasm] (9022525)