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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 loss_of_function via stop_gained

Class:IdFunctionalStatus:2409052
_displayNameloss_of_function via stop_gained
_timestamp2012-07-26 23:26:37
created[InstanceEdit:2409050] Orlic-Milacic, M, 2012-07-17
functionalStatusType[FunctionalStatusType:2426104] loss_of_function
modified[InstanceEdit:2426112] Wu, G, 2012-07-26
structuralVariant[SequenceOntology:2318476] stop_gained
(functionalStatus)[EntityFunctionalStatus:2471684] loss_of_function of OPN1LW LOF variants [photoreceptor disc membrane]
[EntityFunctionalStatus:2471725] loss_of_function of RDH12 LOF variants [photoreceptor inner segment membrane]
[EntityFunctionalStatus:2638178] loss_of_function of p-NICD1 PEST domain mutants [nucleoplasm]
[EntityFunctionalStatus:3304395] loss_of_function of TGFB1:p-TGFBR:ZFYVE9:SMAD2/3 Phosphorylation Motif Mutants [early endosome membrane]
[EntityFunctionalStatus:3311016] loss_of_function of SMAD4 MH2 domain mutants
[EntityFunctionalStatus:3656485] loss_of_function of TGFBR1 KD Mutants:FKBP1A [plasma membrane]
[EntityFunctionalStatus:3656519] loss_of_function of TGFB1:TGFBR2:p-TGFBR1 KD Mutants [plasma membrane]
[EntityFunctionalStatus:3656521] loss_of_function of TGFB1:TGFBR2:TGFBR1 KD Mutants [plasma membrane]
[EntityFunctionalStatus:3656529] loss_of_function of TGFB1:TGFBR2:p-TGFBR1 KD Mutants:ZFYVE9:SMAD2/3 [early endosome membrane]
[EntityFunctionalStatus:3713561] loss_of_function of SMAD2/3 Phosphorylation Motif Mutants [cytosol]
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No pathways have been reviewed or authored by loss_of_function via stop_gained (2409052)