Reactome | MECP2 R306H [nucleoplasm]

Schema > CandidateSet > Entries

candidateOf	[CandidateSet:R-HSA-9005569] MECP2 mutants R306C,(R306H) [nucleoplasm] - Homo sapiens
compartment	[Compartment:7660] nucleoplasm
created	[InstanceEdit:9005571] Orlic-Milacic, Marija, 2017-05-09
crossReference	[DatabaseIdentifier:12020964] Mondo:0010726
dbId	9005555
disease	[Disease:9005548] Rett syndrome
displayName	MECP2 R306H [nucleoplasm]
hasCandidate	[EntityWithAccessionedSequence:R-HSA-9005568] MeCP2_e1 R318H [nucleoplasm] - Homo sapiens
hasMember	[EntityWithAccessionedSequence:R-HSA-9005567] MECP2_e2 R306H [nucleoplasm] - Homo sapiens
inDisease	true
maxDepth	2
name	MECP2 R306H
schemaClass	CandidateSet
species	[Species:48887] Homo sapiens
stId	R-HSA-9005555

(hasCandidate)

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