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Details on Person Jassal, Bijay, 2014-12-23

Class:Id	InstanceEdit:5659745
_displayName	Jassal, Bijay, 2014-12-23
_timestamp	2014-12-23 13:38:32
author	[Person:73447] Jassal, Bijay
dateTime	2014-12-23 18:36:52
(authored)	[FailedReaction:5659734] Defective SLC6A19 does not cotransport neutral amino acids, Na+ from extracellular region to cytosol [Homo sapiens] [FailedReaction:5659755] Defective SLC6A18 does not transport Gly from extracellular region to cytosol [Homo sapiens]
(created)	[EntityWithAccessionedSequence:5659723] SLC6A19 D173N [plasma membrane] [Homo sapiens] [ReplacedResidue:5659724] glycine 496 replaced with L-arginine [Summation:5659725] SLC6A18 encodes a neutral amino acid transporter B(0)AT3 whi... [EntityWithAccessionedSequence:5659726] SLC6A18 G496R [plasma membrane] [Homo sapiens] [EntityFunctionalStatus:5659727] loss_of_function of SLC6A18 mutants [plasma membrane] [EntityWithAccessionedSequence:5659728] SLC6A19 I596Hfs73 [plasma membrane] [Homo sapiens] [Pathway:5659729] Defective SLC6A18 may confer susceptibility to iminoglycinuria and/or hyperglycinuria [Homo sapiens] [FragmentReplacedModification:5659730] Replacement of residues 596 to 667 by HPWLCHLQAHQEPLPEARGPSGAGEHTVHSLHERGPEVLRRPIPRRAIHWCQGRRNQQDLWGGGRAAPACV [DefinedSet:5659731] SLC6A19 mutants [plasma membrane] [Homo sapiens] [EntityWithAccessionedSequence:5659732] SLC6A19 R240 [plasma membrane] [Homo sapiens] List all 34 refering instances
(edited)	[FailedReaction:5659734] Defective SLC6A19 does not cotransport neutral amino acids, Na+ from extracellular region to cytosol [Homo sapiens] [FailedReaction:5659755] Defective SLC6A18 does not transport Gly from extracellular region to cytosol [Homo sapiens]
(modified)	[DefinedSet:375458] neutral amino acids [extracellular region] [Summation:375461] SLC6A19 mediates the uptake of neutral amino acids across th... [Reaction:375473] SLC6A19 cotransports neutral amino acids, Na+ from extracellular region to cytosol [Homo sapiens] [DefinedSet:375481] neutral amino acids [cytosol] [Pathway:5619044] Defective transport of neurotransmitters by SLC6A19 causes Hartnup disorder (HND) [Homo sapiens] [Pathway:5619079] Defective SLC6A18 may confer susceptibility to iminoglycinuria and/or hyperglycinuria [Homo sapiens] [Pathway:5619102] SLC transporter disorders [Homo sapiens] [Summation:5653851] SLC36A2 encodes proton-coupled amino acid transporter 2 (PAT... [Summation:5653858] SLC36A2 encodes proton-coupled amino acid transporter 2 (PAT...
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No pathways have been reviewed or authored by Jassal, Bijay, 2014-12-23 (5659745)