Reactome | Essential pentosuria

Schema > Pathway > Entries

authored	[InstanceEdit:5678684] D'Eustachio, Peter, 2015-02-25
created	[InstanceEdit:5662852] D'Eustachio, Peter, 2015-01-13
crossReference	[DatabaseIdentifier:12020935] Mondo:0019214
dbId	5662853
disease	[Disease:5656463] carbohydrate metabolic disorder
displayName	Essential pentosuria
edited	[InstanceEdit:5678684] D'Eustachio, Peter, 2015-02-25
eventOf	[Pathway:R-HSA-5663084] Diseases of carbohydrate metabolism - Homo sapiens
hasDiagram	true
hasEHLD	false
hasEvent	[FailedReaction:R-HSA-5662851] Defective DCXR does not reduce L-xylulose to xylitol - Homo sapiens
isInDisease	true
isInferred	false
lastUpdatedDate	2019-03-25
literatureReference	[LiteratureReference:5660062] Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuria [LiteratureReference:5660043] The enzymatic defect in essential pentosuria
maxDepth	2
modified	[InstanceEdit:9847082] Weiser, Joel, 2023-10-12
name	Essential pentosuria
normalPathway	[Pathway:R-HSA-5661270] Formation of xylulose-5-phosphate
releaseDate	2015-09-22
reviewStatus	[ReviewStatus:9821382] five stars
reviewed	[InstanceEdit:6791051] Jassal, Bijay, 2015-08-17
schemaClass	Pathway
species	[Species:48887] Homo sapiens
stId	R-HSA-5662853
summation	[Summation:5662850] Essential pentosuria, the excretion in the urine of high lev...
updateTrackers	[UpdateTracker:9778624] Update Tracker - [Pathway:5662853] Essential pentosuria - v68:[updateContainedRLE]

(updatedInstance)	[UpdateTracker:9778624] Update Tracker - [Pathway:5662853] Essential pentosuria - v68:[updateContainedRLE]
(hasEvent)	[Pathway:R-HSA-5663084] Diseases of carbohydrate metabolism

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