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MECP2 P304R [nucleoplasm]
Stable Identifier
R-HSA-9005538
Type
Set [CandidateSet]
Species
Homo sapiens
Compartment
nucleoplasm
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Disorders of Developmental Biology (Homo sapiens)
Disorders of Nervous System Development (Homo sapiens)
Pervasive developmental disorders (Homo sapiens)
Loss of function of MECP2 in Rett syndrome (Homo sapiens)
Loss of MECP2 binding ability to the NCoR/SMRT complex (Homo sapiens)
MECP2 mutants P302R,K304E,K305R,R306C,(R306H) do not bind NCoR/SMRT complex (Homo sapiens)
MECP2 mutants P302R,K304E,K305R,R306C,(R306H) [nucleoplasm] (Homo sapiens)
MECP2 P304R [nucleoplasm] (Homo sapiens)
Participants
members
MECP2_e2 P302R [nucleoplasm]
(Homo sapiens)
candidates
MeCP2_e1 P314R [nucleoplasm]
(Homo sapiens)
Participates
as a member of
MECP2 mutants P302R,K304E,K305R,R306C,(R306H) [nucleoplasm] (Homo sapiens)
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