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 SLC4A1 V488M [plasma membrane]
| Class:Id | EntityWithAccessionedSequence:5657845 |
|---|---|
| _displayName | SLC4A1 V488M [plasma membrane] |
| _timestamp | 2015-09-04 19:49:36 |
| compartment | [Compartment:876] plasma membrane |
| created | [InstanceEdit:5657850] Jassal, Bijay, 2014-12-16 |
| disease | [Disease:5656223] hereditary spherocytosis |
| endCoordinate | 911 |
| hasModifiedResidue | [ReplacedResidue:5657811] L-valine 488 replaced with L-methionine |
| name | SLC4A1 V488M Band 3 anion transport protein B3AT_HUMAN |
| referenceEntity | [ReferenceGeneProduct:50605] UniProt:P02730 SLC4A1 [Homo sapiens] |
| species | [Species:48887] Homo sapiens |
| stableIdentifier | [StableIdentifier:6795758] R-HSA-5657845.1 |
| startCoordinate | 1 |
| (hasMember) | [DefinedSet:5657826] SLC4A1 mutants [plasma membrane] [Homo sapiens] |
| [Change default viewing format] | |
No pathways have been reviewed or authored by SLC4A1 V488M [plasma membrane] (5657845)
