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Details on Person Jassal, Bijay, 2014-12-01

Class:Id	InstanceEdit:5653590
_displayName	Jassal, Bijay, 2014-12-01
_timestamp	2014-12-01 15:59:04
author	[Person:73447] Jassal, Bijay
dateTime	2014-12-01 20:57:56
(authored)	[FailedReaction:5653596] Defective SLC35C1 does not transport UDP-Fuc from cytosol to Golgi lumen [Homo sapiens] [FailedReaction:5653622] Defective SLC35A3 does not exchange UDP-GlcNAc for UMP [Homo sapiens]
(created)	[EntityWithAccessionedSequence:5653584] SLC35A3 S296G [Golgi membrane] [Homo sapiens] [Person:5653585] Lee, Jack [ReplacedResidue:5653586] L-serine 296 replaced with glycine [Summation:5653587] The human gene SLC35A3 encodes a UDP-GlcNAc transporter. It ... [Person:5653588] Jalas, Chaim [Summation:5653589] The human gene SLC35A3 encodes a UDP-GlcNAc transporter. It ... [Summation:5653591] The human gene SLC35C1 encodes a GDP-fucose transporter that... [LiteratureReference:5653592] Congenital disorder of fucosylation type 2c (LADII) presenting with short stature and developmental delay with minimal adhesion defect [EntityWithAccessionedSequence:5653593] SLC35C1 E31* [Golgi membrane] [Homo sapiens] [EntityWithAccessionedSequence:5653594] SLC35C1 T308* [Golgi membrane] [Homo sapiens] List all 38 refering instances
(edited)	[FailedReaction:5653596] Defective SLC35C1 does not transport UDP-Fuc from cytosol to Golgi lumen [Homo sapiens] [FailedReaction:5653622] Defective SLC35A3 does not exchange UDP-GlcNAc for UMP [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) [Summation:741445] The human gene SLC35A3 encodes a UDP-GlcNAc transporter (Ish... [Reaction:741450] SLC35A3 exchanges UDP-GlcNAc for UMP [Homo sapiens] [Reaction:742345] SLC35C1 transports GDP-Fuc from cytosol to Golgi lumen [Homo sapiens] [Summation:742371] SLC35C1 encodes a GDP-fucose transporter that resides on the... [Pathway:5619078] Defective SLC35C1 causes congenital disorder of glycosylation 2C (CDG2C) [Homo sapiens] [Pathway:5619083] Defective SLC35A3 causes arthrogryposis, mental retardation, and seizures (AMRS) [Homo sapiens]
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No pathways have been reviewed or authored by Jassal, Bijay, 2014-12-01 (5653590)