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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 SMAD4 D351H [cytosol]

Class:IdEntityWithAccessionedSequence:3310965
_displayNameSMAD4 D351H [cytosol]
_timestamp2013-09-05 12:24:26
compartment[Compartment:70101] cytosol
created[InstanceEdit:3310962] Orlic-Milacic, M, 2013-04-24
crossReference[DatabaseIdentifier:3310968] COSMIC:COSV61684645
disease[Disease:1500689] cancer
[Disease:1248674] large intestine cancer
[Disease:1500575] ovarian cancer
[Disease:2328198] pancreatic cancer
[Disease:1500699] lung cancer
endCoordinate552
hasModifiedResidue[ReplacedResidue:3310966] L-aspartic acid 351 replaced with L-histidine
literatureReference[LiteratureReference:3318202] A structural basis for mutational inactivation of the tumour suppressor Smad4
[LiteratureReference:3304374] SMAD2, SMAD3 and SMAD4 mutations in colorectal cancer
modified[InstanceEdit:3318205] Orlic-Milacic, M, 2013-04-25
nameSMAD4 D351H
SMAD4 Asp351His
referenceEntity[ReferenceGeneProduct:64628] UniProt:Q13485 SMAD4 [Homo sapiens]
species[Species:48887] Homo sapiens
stableIdentifier[StableIdentifier:4545902] R-HSA-3310965.1
startCoordinate1
(hasMember)[CandidateSet:3311017] SMAD4 MH2 domain mutants [cytosol] [Homo sapiens]
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No pathways have been reviewed or authored by SMAD4 D351H [cytosol] (3310965)