Reactome: A Curated Pathway Database
THIS SITE IS USED FOR CURATION AND TESTING
IT IS NOT STABLE, IS LINKED TO AN INCOMPLETE DATA SET, AND IS NOT MONITORED FOR PERFORMANCE. WE STRONGLY RECOMMEND THE USE OF OUR PUBLIC SITE

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.

If you have an ORCID ID that is not listed on this page, please forward this information to us and we will update your Reactome pathway records.

Name Email address

Details on Person Jassal, Bijay, 2014-11-21

Class:IdInstanceEdit:5649739
_displayNameJassal, Bijay, 2014-11-21
_timestamp2014-11-21 09:13:56
author[Person:73447] Jassal, Bijay
dateTime2014-11-21 14:12:25
(authored)[FailedReaction:5649742] Defective SLC33A1 does not transport Ac-CoA from cytosol to Golgi lumen [Homo sapiens]
(created)[Summation:5649737] The human gene SLC33A1 encodes acetyl-CoA transporter AT1. S...
[Disease:5649738] neurodegenerative disease
[Disease:5649740] myopathy
[Disease:5649741] cataract
[FailedReaction:5649742] Defective SLC33A1 does not transport Ac-CoA from cytosol to Golgi lumen [Homo sapiens]
(edited)[FailedReaction:5649742] Defective SLC33A1 does not transport Ac-CoA from cytosol to Golgi lumen [Homo sapiens]
(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)
[CatalystActivity:727756] acetyl-CoA transmembrane transporter activity of SLC33A1 [Golgi membrane]
[Reaction:727759] SLC33A1 transports Ac-CoA from cytosol to Golgi lumen [Homo sapiens]
[EntityWithAccessionedSequence:2219571] NAGLU R643C [lysosomal lumen] [Homo sapiens]
[DefinedSet:2565899] RHO Class I mutants [photoreceptor disc membrane] [Homo sapiens]
[EntityWithAccessionedSequence:2565900] RHO R135L [photoreceptor disc membrane] [Homo sapiens]
[EntityWithAccessionedSequence:2565901] RHO P347L [photoreceptor disc membrane] [Homo sapiens]
[EntityWithAccessionedSequence:2565904] RHO P347S [photoreceptor disc membrane] [Homo sapiens]
[EntityWithAccessionedSequence:2565908] RHO G51V [photoreceptor disc membrane] [Homo sapiens]
[EntityWithAccessionedSequence:2565909] RHO R135W [photoreceptor disc membrane] [Homo sapiens]
List all 123 refering instances
[Change default viewing format]
No pathways have been reviewed or authored by Jassal, Bijay, 2014-11-21 (5649739)
Follow Reactome