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Details on Person Jassal, Bijay, 2014-09-17

Class:Id	InstanceEdit:5623578
_displayName	Jassal, Bijay, 2014-09-17
_timestamp	2014-09-17 15:39:42
author	[Person:73447] Jassal, Bijay
dateTime	2014-09-17 19:38:09
(authored)	[FailedReaction:5623558] Defective SLC11A2 does not cotransport Fe2+, H+ from extracellular region to cytosol [Homo sapiens] [FailedReaction:5623588] Defective SLC12A1 does not cotransport Na+, K+, 2Cl- from extracellular region to cytosol [Homo sapiens]
(created)	[ReplacedResidue:5623548] L-valine 278 replaced with L-phenylalanine [Person:5623549] Punzi, Leonardo [Person:5623550] Madrigal, G [Person:5623551] Okubo, Y [NonsenseMutation:5623552] Nonsense mutation at L-tryptophan 625 [Person:5623553] Karet, F E [ReplacedResidue:5623554] L-arginine 302 replaced with L-glutamine [Disease:5623555] Rh deficiency syndrome [Person:5623556] Simon, D B [LiteratureReference:5623557] Miscellaneous non-inflammatory musculoskeletal conditions. Bartter's and Gitelman's diseases List all 60 refering instances
(edited)	[FailedReaction:5623558] Defective SLC11A2 does not cotransport Fe2+, H+ from extracellular region to cytosol [Homo sapiens] [FailedReaction:5623588] Defective SLC12A1 does not cotransport Na+, K+, 2Cl- from extracellular region to cytosol [Homo sapiens]
(modified)	[Reaction:426086] SLC12A1,2 cotransports Na+, K+, 2Cl- from extracellular region to cytosol [Homo sapiens] [CatalystActivity:426140] sodium:potassium:chloride symporter activity of SLC12A1,2 [plasma membrane] [DefinedSet:426153] SLC12A1,2 [plasma membrane] [Homo sapiens] [Summation:435343] The primary site for absorption of dietary iron is the duode... [CatalystActivity:435344] iron ion transmembrane transporter activity of SLC11A2 [plasma membrane] [Reaction:435349] SLC11A2 cotransports Fe2+, H+ from extracellular region to cytosol [Homo sapiens] [Pathway:5619042] Defective RHAG causes regulator type Rh-null hemolytic anemia (RHN) [Homo sapiens] [Pathway:5619048] Defective SLC11A2 causes hypochromic microcytic anemia, with iron overload 1 (AHMIO1) [Homo sapiens] [Pathway:5619056] Defective HK1 causes hexokinase deficiency (HK deficiency) [Homo sapiens] [Pathway:5619060] Defective CP causes aceruloplasminemia (ACERULOP) [Homo sapiens] List all 20 refering instances
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No pathways have been reviewed or authored by Jassal, Bijay, 2014-09-17 (5623578)