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 NHLRC1 C26S [cytosol]
| Class:Id | EntityWithAccessionedSequence:3797231 |
|---|---|
| _displayName | NHLRC1 C26S [cytosol] |
| _timestamp | 2014-11-20 03:54:25 |
| compartment | [Compartment:70101] cytosol |
| created | [InstanceEdit:3797222] D'Eustachio, P, 2013-07-05 |
| disease | [Disease:3229130] glycogen storage disease |
| endCoordinate | 395 |
| hasModifiedResidue | [ReplacedResidue:3797229] L-cysteine 26 replaced with L-serine |
| literatureReference | [LiteratureReference:3797223] Mutations in NHLRC1 cause progressive myoclonus epilepsy |
| modified | [InstanceEdit:3797234] D'Eustachio, P, 2013-07-05 [InstanceEdit:3828059] D'Eustachio, P, 2013-07-09 |
| name | NHLRC1 C26S E3 ubiquitin-protein ligase NHLRC1 C26S malin C26S EMP2B C26S |
| referenceEntity | [ReferenceGeneProduct:151042] UniProt:Q6VVB1 NHLRC1 [Homo sapiens] |
| species | [Species:48887] Homo sapiens |
| stableIdentifier | [StableIdentifier:5647646] R-HSA-3797231.1 |
| startCoordinate | 1 |
| (hasMember) | [DefinedSet:3797212] NHLRC1 mutants [cytosol] [Homo sapiens] |
| [Change default viewing format] | |
No pathways have been reviewed or authored by NHLRC1 C26S [cytosol] (3797231)
