Query author contributions in Reactome

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Details on Person gangliosidosis GM2

Class:Id	Disease:3656251
_displayName	gangliosidosis GM2
_timestamp	2013-05-31 11:01:02
created	[InstanceEdit:3656245] Jassal, B, 2013-05-31
identifier	3321
name	gangliosidosis GM2
referenceDatabase	[ReferenceDatabase:1247631] DOID
synonym	GM>2< gangliosidosis (disorder)
(disease)	[Pathway:3656248] Defective HEXB causes GM2G2 (Hyaluronan metabolism) [Homo sapiens] [FailedReaction:3662344] Defective HEXB does not cleave the terminal GalNAc from DS [Homo sapiens] [FailedReaction:9035982] Defective HEXB does not cleave the terminal GalNAc from HA fragments [Homo sapiens] [FailedReaction:9035983] Defective HEXB does not cleave the terminal GalNAc from keratan sulfate [Homo sapiens] [Pathway:9953282] Defective HEXB causes GM2G2 (CS/DS degradation) [Homo sapiens] [Pathway:9953284] Defective HEXB causes GM2G2 (Keratan metabolism) [Homo sapiens] [EntityWithAccessionedSequence:3700843] HEXB M26Cfs5 [lysosomal lumen] [Homo sapiens] [EntityWithAccessionedSequence:3700889] HEXB I322Kfs5 [lysosomal lumen] [Homo sapiens] [EntityWithAccessionedSequence:3700901] HEXB S62L [lysosomal lumen] [Homo sapiens] [EntityWithAccessionedSequence:3700930] HEXB R284* [lysosomal lumen] [Homo sapiens]
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No pathways have been reviewed or authored by gangliosidosis GM2 (3656251)