Reactome Pathway Database

Schema > EntityWithAccessionedSequence > Entries

SGSH S66W [lysosomal lumen] Show undefined attributes

compartment

[Compartment:161320] lysosomal lumen

created [InstanceEdit:2214338] Jassal, B, 2012年04月30日

crossReference

[DatabaseIdentifier:11945073] 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年06月07日

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

Referrals

(updatedInstance)

(hasMember)

[DefinedSet:R-HSA-2214337] SGSH mutants [lysosomal lumen]

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