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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 Jassal, Bijay, 2014-11-27

Class:IdInstanceEdit:5652118
_displayNameJassal, Bijay, 2014-11-27
_timestamp2014-11-27 15:52:04
author[Person:73447] Jassal, Bijay
dateTime2014-11-27 20:50:16
(created)[Person:5652085] Szybowska, Marta
[FragmentReplacedModification:5652086] Replacement of residues 324 to 347 by LPLALDSSLVLSTSTAFPEVQPKP
[Person:5652087] Eroshkin, Alexey
[EntityWithAccessionedSequence:5652088] SLC35A2 F324Lfs*25 [Golgi membrane] [Homo sapiens]
[Person:5652089] Turner, Emily H
[Person:5652090] Smith, Joshua D
[Person:5652091] Yuasa, Isao
[Person:5652092] Iai, Mizue
[EntityWithAccessionedSequence:5652093] SLC35A2 V331I [Golgi membrane] [Homo sapiens]
[Person:5652094] Hayasaka, Kiyoshi
List all 45 refering instances
(modified)[PathwayDiagram:601857] Diagram of Transport of vitamins, nucleosides, and related molecules, Defective SLC27A4 causes ichthyosis prematurity syndrome (IPS), Defective SLC29A3 causes histiocytosis-lymphadenopathy plus syndrome (HLAS), Defective SLC33A1 causes spastic paraplegia 42 (SPG42), Defective SLC35A2 causes congenital disorder of glycosylation 2M (CDG2M), Defective SLC35A3 causes arthrogryposis, mental retardation, and seizures (AMRS), Defective SLC35C1 causes congenital disorder of glycosylation 2C (CDG2C), and Defective SLC35A1 causes congenital disorder of glycosylation 2F (CDG2F)
[Summation:735681] The human gene SLC35A2 encodes the UDP-galactose transporter...
[DefinedSet:735691] UDP-Gal, UDP-GalNAc [Golgi lumen]
[DefinedSet:735692] UDP-Gal, UDP-GalNAc [cytosol]
[Reaction:735702] SLC35A2 exchanges UDP-Gal, UDP-GalNAc for UMP [Homo sapiens]
[Pathway:5619072] Defective SLC35A2 causes congenital disorder of glycosylation 2M (CDG2M) [Homo sapiens]
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No pathways have been reviewed or authored by Jassal, Bijay, 2014-11-27 (5652118)
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