Query author contributions in Reactome

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Details on Person Jassal, Bijay, 2014-06-13

Class:Id	InstanceEdit:5601814
_displayName	Jassal, Bijay, 2014-06-13
_timestamp	2014-06-13 12:37:45
author	[Person:73447] Jassal, Bijay
dateTime	2014-06-13 16:35:35
(authored)	[FailedReaction:5601843] Defective CYP17A1 does not 17-hydroxylate PREG [Homo sapiens] [FailedReaction:5601849] Defective CYP19A1 does not convert ANDST to E1 [Homo sapiens] [FailedReaction:9035954] Defective CYP17A1 does not 17-hydroxylate P4 [Homo sapiens] [FailedReaction:9035956] Defective CYP17A1 does not cleave 17aHPROG [Homo sapiens]
(created)	[Person:5601753] Gore, M E [LiteratureReference:5601755] A novel point mutation in P450c17 (CYP17) causing combined 17alpha-hydroxylase/17,20-lyase deficiency [EntityWithAccessionedSequence:5601756] CYP17A1 R96Q [endoplasmic reticulum membrane] [Homo sapiens] [ReplacedResidue:5601757] L-arginine 96 replaced with L-glutamine [Person:5601758] Mailloux, J [Person:5601759] Brooke, A M [Person:5601760] Moore, C C [Person:5601761] Grumbach, M M [Person:5601762] Yanase, T [LiteratureReference:5601763] Molecular basis of 17?-hydroxylase/17,20-lyase deficiency List all 115 refering instances
(edited)	[FailedReaction:5601843] Defective CYP17A1 does not 17-hydroxylate PREG [Homo sapiens] [FailedReaction:5601849] Defective CYP19A1 does not convert ANDST to E1 [Homo sapiens] [FailedReaction:9035954] Defective CYP17A1 does not 17-hydroxylate P4 [Homo sapiens] [FailedReaction:9035956] Defective CYP17A1 does not cleave 17aHPROG [Homo sapiens]
(modified)	[Reaction:193060] CYP19A1 hydroxylates ANDST to E1 [Homo sapiens] [Reaction:193068] CYP17A1 17-hydroxylates PREG [Homo sapiens] [Reaction:193072] CYP17A1 17-hydroxylates P4 to 17aHPROG [Homo sapiens] [SimpleEntity:193079] ANDST [cytosol] [SimpleEntity:193092] 17aHPROG [cytosol] [Reaction:193099] CYP17A1 cleaves 17aHPROG to ANDST [Homo sapiens] [Summation:196396] The conversion of androstenedione (ANDST) to estrone (E1) is... [PathwayDiagram:500339] Diagram of Phase I - Functionalization of compounds, Defective CYP11A1 causes AICSR, Defective CYP11B1 causes AH4, Defective CYP11B2 causes CMO-1 deficiency, Defective CYP19A1 causes AEXS, Defective CYP1B1 causes Glaucoma, Defective CYP21A2 causes AH3, Defective CYP24A1 causes HCAI, Defective CYP26B1 causes RHFCA, Defective CYP26C1 causes FFDD4, Defective CYP2U1 causes SPG56, Defective CYP4F22 causes ARCI5, Defective CYP7B1 causes SPG5A and CBAS3, Defective FMO3 causes TMAU, Defective MAOA causes BRUNS, and Defective TBXAS1 causes GHDD [PathwayDiagram:500771] Diagram of Phase II - Conjugation of compounds, Defective AHCY causes HMAHCHD, Defective GCLC causes HAGGSD, Defective GGT1 causes GLUTH, Defective GSS causes GSS deficiency, Defective MAT1A causes MATD, Defective OPLAH causes OPLAHD, Defective SLC35D1 causes SCHBCKD, and Defective TPMT causes TPMT deficiency [PathwayDiagram:5424635] Diagram of Aflatoxin activation and detoxification, Defective ACY1 causes encephalopathy, and Defective GGT1 causes GLUTH List all 13 refering instances
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No pathways have been reviewed or authored by Jassal, Bijay, 2014-06-13 (5601814)