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, B, 2013-11-04

Class:IdInstanceEdit:4839807
_displayNameJassal, B, 2013-11-04
_timestamp2013-11-04 09:53:43
author[Person:73447] Jassal, Bijay
dateTime2013-11-04 14:52:39
(created)[ReplacedResidue:4839777] L-serine 290 replaced with L-phenylalanine
[LiteratureReference:4839778] Mutations in the alpha 1,2-mannosidase gene, MAN1B1, cause autosomal-recessive intellectual disability
[EntityWithAccessionedSequence:4839779] MOGS F652L [endoplasmic reticulum membrane] [Homo sapiens]
[Person:4839780] Khan, Muzammil Ahmad
[Person:4839781] Salih, Mustafa A
[Person:4839782] Tan, J
[Person:4839783] Vincent, John B
[EntityWithAccessionedSequence:4839784] MGAT2 K237N [Golgi membrane] [Homo sapiens]
[Person:4839785] Vincent, J B
[Summation:4839786] Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminylt...
List all 66 refering instances
(modified)[PathwayDiagram:548980] Diagram of Asparagine N-linked glycosylation, Defective ALG1 causes CDG-1k, Defective ALG11 causes CDG-1p, Defective ALG2 causes CDG-1i, Defective DPAGT1 causes CDG-1j, CMSTA2, Defective GFPT1 causes CMSTA1, Defective MPI causes MPI-CDG, Defective PMM2 causes PMM2-CDG, Defective ALG12 causes CDG-1g, Defective ALG3 causes CDG-1d, Defective ALG6 causes CDG-1c, Defective ALG8 causes CDG-1h, Defective ALG9 causes CDG-1l, Defective DPM1 causes DPM1-CDG, Defective DPM2 causes DPM2-CDG, Defective DPM3 causes DPM3-CDG, Defective MPDU1 causes CDG-1f, Defective RFT1 causes CDG-1n, Defective DHDDS causes RP59, Defective DOLK causes DOLK-CDG, Defective SRD5A3 causes SRD5A3-CDG, KHRZ, Defective B4GALT1 causes CDG-2d, Defective MAN1B1 causes MRT15, Defective MGAT2 causes CDG-2a, Defective MOGS causes CDG-2b, and Defective ALG14 causes ALG14-CMS
[Summation:901023] Proteins that are released from the CNX or CRT complex with ...
[Summation:1015746] The addition of a GlcNAc on the alpha-1,6 mannose on the alp...
[Summation:3656433] The family of beta 4-galactosyltransferases (B4GALTs) is com...
[PathwayDiagram:4551365] Diagram of Diseases associated with N-glycosylation of proteins
[FailedReaction:4793947] Defective MOGS does not cleave glucose from an N-glycosylated protein [Homo sapiens]
[Pathway:4793950] Defective MAN1B1 causes MRT15 [Homo sapiens]
[Pathway:4793952] Defective MGAT2 causes CDG-2a [Homo sapiens]
[Pathway:4793953] Defective B4GALT1 causes CDG-2d [Homo sapiens]
[Pathway:4793954] Defective MOGS causes CDG-2b [Homo sapiens]
List all 12 refering instances
[Change default viewing format]
No pathways have been reviewed or authored by Jassal, B, 2013-11-04 (4839807)