Reactome: A Curated Pathway Database
THIS SITE IS USED FOR CURATION AND TESTING
IT IS NOT STABLE, IS LINKED TO AN INCOMPLETE DATA SET, AND IS NOT MONITORED FOR PERFORMANCE. WE STRONGLY RECOMMEND THE USE OF OUR PUBLIC SITE

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.

If you have an ORCID ID that is not listed on this page, please forward this information to us and we will update your Reactome pathway records.

Name Email address

Details on Person A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome

Class:IdLiteratureReference:9005560
_displayNameA previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome
_timestamp2017-05-09 13:47:35
author[Person:9005547] Mnatzakanian, Gevork N
[Person:5682757] Lohi, Hannes
[Person:3797213] Munteanu, Iulia
[Person:9005543] Alfred, Simon E
[Person:9005579] Yamada, Takahiro
[Person:9005546] MacLeod, Patrick J M
[Person:9005532] Jones, Julie R
[Person:372472] Scherer, SW
[Person:9005559] Schanen, N Carolyn
[Person:5661017] Friez, Michael J
[Person:4839783] Vincent, John B
[Person:3785657] Minassian, Berge A
created[InstanceEdit:9005571] Orlic-Milacic, Marija, 2017-05-09
journalNat. Genet.
pages339-41
pubMedIdentifier15034579
titleA previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome
volume36
year2004
(literatureReference)[Pathway:8986944] Transcriptional Regulation by MECP2 [Homo sapiens]
[EntityWithAccessionedSequence:9005539] MECP2_e1 [nucleoplasm] [Homo sapiens]
[EntityWithAccessionedSequence:9005541] MeCP2_e1 K317R [nucleoplasm] [Homo sapiens]
[EntityWithAccessionedSequence:9005542] MECP2_e2 R306C [nucleoplasm] [Homo sapiens]
[EntityWithAccessionedSequence:9005563] MECP2_e2 K305R [nucleoplasm] [Homo sapiens]
[EntityWithAccessionedSequence:9005567] MECP2_e2 R306H [nucleoplasm] [Homo sapiens]
[EntityWithAccessionedSequence:9005568] MeCP2_e1 R318H [nucleoplasm] [Homo sapiens]
[EntityWithAccessionedSequence:9005573] MECP2_e2 [nucleoplasm] [Homo sapiens]
[EntityWithAccessionedSequence:9005574] MeCP2_e1 P314R [nucleoplasm] [Homo sapiens]
[EntityWithAccessionedSequence:9005576] MECP2_e2 K304E [nucleoplasm] [Homo sapiens]
List all 19 refering instances
[Change default viewing format]
No pathways have been reviewed or authored by A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome (9005560)