Reactome | MECP2_e2 S134F [nucleoplasm]

Schema > EntityWithAccessionedSequence > Entries

compartment	[Compartment:7660] nucleoplasm
created	[InstanceEdit:9022505] Orlic-Milacic, Marija, 2017-09-25
crossReference	[DatabaseIdentifier:12020964] Mondo:0010726
dbId	9022506
disease	[Disease:9005548] Rett syndrome
displayName	MECP2_e2 S134F [nucleoplasm]
endCoordinate	486
hasModifiedResidue	[ReplacedResidue:9022508] L-serine 134 replaced with L-phenylalanine
inDisease	true
maxDepth	1
memberOf	[CandidateSet:R-HSA-9022504] MECP2 S134F [nucleoplasm] - Homo sapiens
modified	[InstanceEdit:9022529] Orlic-Milacic, Marija, 2017-09-25
name	MECP2_e2 S134F MECP2A S134F
referenceEntity	[ReferenceIsoform:uniprot:P51608-1] UniProt:P51608-1 MECP2
referenceType	ReferenceIsoform
schemaClass	EntityWithAccessionedSequence
species	[Species:48887] Homo sapiens
stId	R-HSA-9022506
startCoordinate	1

(hasMember)

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