Reactome: A Curated Pathway Database
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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 SLC2A1 K256V [plasma membrane]

Class:IdEntityWithAccessionedSequence:5632870
_displayNameSLC2A1 K256V [plasma membrane]
_timestamp2015-09-04 19:47:47
compartment[Compartment:876] plasma membrane
created[InstanceEdit:5632829] Jassal, Bijay, 2014-10-29
disease[Disease:5632824] early infantile epileptic encephalopathy
endCoordinate492
hasModifiedResidue[ReplacedResidue:5632777] L-lysine 256 replaced with L-valine
literatureReference[LiteratureReference:70157] Mammalian facilitative glucose transporter family: structure and molecular regulation
[LiteratureReference:70141] Structural analysis of the GLUT1 facilitative glucose transporter (review).
nameSLC2A1 K256V
GLUT1
Solute carrier family 2, facilitated glucose transporter, member 1
Glucose transporter type 1, erythrocyte/brain
HepG2 glucose transporter
referenceEntity[ReferenceGeneProduct:56064] UniProt:P11166 SLC2A1 [Homo sapiens]
species[Species:48887] Homo sapiens
stableIdentifier[StableIdentifier:6795665] R-HSA-5632870.1
startCoordinate1
(hasMember)[DefinedSet:5632862] SLC2A1 mutants [plasma membrane] [Homo sapiens]
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No pathways have been reviewed or authored by SLC2A1 K256V [plasma membrane] (5632870)