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MECP2 T158A:SIN3A:HDAC1 [nucleoplasm]
Stable Identifier
R-HSA-9023459
Type
Complex
Species
Homo sapiens
Compartment
nucleoplasm
Locations in the PathwayBrowser
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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 5mC-DNA (Homo sapiens)
MECP2 T158A:SIN3A complex does not bind BDNF gene promoter (Homo sapiens)
MECP2 T158A:SIN3A:HDAC1 [nucleoplasm] (Homo sapiens)
Participants
components
MECP2 T158A [nucleoplasm]
(Homo sapiens)
SIN3A:HDAC1 homodimer [nucleoplasm]
(Homo sapiens)
Participates
as an input of
MECP2 T158A:SIN3A complex does not bind BDNF gene promoter (Homo sapiens)
Disease
Name
Identifier
Synonyms
Rett syndrome
DOID:1206
Rett's disorder, cerebroatrophic hyperammonemia
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