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 SLC22A5 R254* [plasma membrane]
| Class:Id | EntityWithAccessionedSequence:5625665 |
|---|---|
| _displayName | SLC22A5 R254* [plasma membrane] |
| _timestamp | 2015-09-04 19:47:02 |
| compartment | [Compartment:876] plasma membrane |
| created | [InstanceEdit:5625621] Jassal, Bijay, 2014-10-06 |
| disease | [Disease:5625675] systemic primary carnitine deficiency disease |
| endCoordinate | 557 |
| hasModifiedResidue | [NonsenseMutation:5625616] Nonsense mutation at L-arginine 254 |
| name | SLC22A5 R254* OCTN2 Organic cation transporter 2 solute carrier family 22 (organic cation transporter), member 5 Solute carrier family 22 member 5 S22A5_HUMAN |
| referenceEntity | [ReferenceGeneProduct:60848] UniProt:O76082 SLC22A5 [Homo sapiens] |
| species | [Species:48887] Homo sapiens |
| stableIdentifier | [StableIdentifier:6795622] R-HSA-5625665.1 |
| startCoordinate | 1 |
| (hasMember) | [DefinedSet:5625715] SLC22A5 mutants [plasma membrane] [Homo sapiens] |
| [Change default viewing format] | |
No pathways have been reviewed or authored by SLC22A5 R254* [plasma membrane] (5625665)
