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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 PALB2 Q988* [nucleoplasm]

Class:IdEntityWithAccessionedSequence:9704801
_displayNamePALB2 Q988* [nucleoplasm]
_timestamp2020-10-15 11:36:14
compartment[Compartment:7660] nucleoplasm
created[InstanceEdit:9704804] Orlic-Milacic, Marija, 2020-10-14
crossReference[DatabaseIdentifier:9704907] ClinGen:CA164468
disease[Disease:9704435] Fanconi anemia
[Disease:1500689] cancer
endCoordinate987
hasModifiedResidue[NonsenseMutation:9704803] Nonsense mutation at L-glutamine 988
literatureReference[LiteratureReference:9704776] Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer
modified[InstanceEdit:9704911] Orlic-Milacic, Marija, 2020-10-15
namePALB2 Q988*
PALB2 Gln988*
PALB2 Q988TER
PALB2 Gln988TER
referenceEntity[ReferenceGeneProduct:241569] UniProt:Q86YC2 PALB2 [Homo sapiens]
species[Species:48887] Homo sapiens
stableIdentifier[StableIdentifier:9704811] R-HSA-9704801.1
startCoordinate1
(hasCandidate)[CandidateSet:9704406] PALB2 mutants (BRCA2/RAD51/RAD51C binding) [nucleoplasm] [Homo sapiens]
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No pathways have been reviewed or authored by PALB2 Q988* [nucleoplasm] (9704801)