Reactome | SGSH S66W [lysosomal lumen]

Schema > EntityWithAccessionedSequence > Entries

compartment	[Compartment:161320] lysosomal lumen
created	[InstanceEdit:2214338] Jassal, B, 2012-04-30
crossReference	[DatabaseIdentifier:12020937] Mondo:0018937
dbId	2214340
disease	[Disease:2226064] mucopolysaccharidosis III
displayName	SGSH S66W [lysosomal lumen]
endCoordinate	502
hasModifiedResidue	[ReplacedResidue:2214342] L-serine 66 replaced with L-tryptophan
inDisease	true
maxDepth	1
memberOf	[DefinedSet:R-HSA-2214337] SGSH mutants [lysosomal lumen] - Homo sapiens
modified	[InstanceEdit:3662298] Jassal, B, 2013-06-07
name	SGSH S66W N-sulphoglucosamine sulphohydrolase SPHM_HUMAN p.Ser66Trp SGSH
referenceEntity	[ReferenceGeneProduct:uniprot:P51688] UniProt:P51688 SGSH
referenceType	ReferenceGeneProduct
schemaClass	EntityWithAccessionedSequence
species	[Species:48887] Homo sapiens
stId	R-HSA-2214340
startCoordinate	21
updateTrackers	[UpdateTracker:9888300] Update Tracker - [EntityWithAccessionedSequence:2214340] SGSH S66W [lysosomal lumen] - v46:[modifyName] [UpdateTracker:9874452] Update Tracker - [EntityWithAccessionedSequence:2214340] SGSH S66W [lysosomal lumen] - v43:[modifyName]

(updatedInstance)	[UpdateTracker:9888300] Update Tracker - [EntityWithAccessionedSequence:2214340] SGSH S66W [lysosomal lumen] - v46:[modifyName] [UpdateTracker:9874452] Update Tracker - [EntityWithAccessionedSequence:2214340] SGSH S66W [lysosomal lumen] - v43:[modifyName]
(hasMember)	[DefinedSet:R-HSA-2214337] SGSH mutants [lysosomal lumen]

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