Loss of function of MECP2 in Rett syndrome - Wikidata - awgldk - TriplyDB

Loss of function of MECP2 in Rett syndrome

Loss of function of MECP2 in Rett syndrome

http://www.wikidata.org/entity/Q56860940

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Pervasive developmental disorders

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Loss of function of MECP2 in Rett syndrome

http://www.wikidata.org/entity/Q56860940

description

An instance of the biological ...... Rett syndrome in Homo sapiens

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name

Loss of function of MECP2 in Rett syndrome

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type

label

Loss of function of MECP2 in Rett syndrome

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Loss of function of MECP2 in Rett syndrome

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Rett syndrome: genes, synapses, circuits, and therapeutics

Activity-dependent neuronal signalling and autism spectrum disorder.

Rett syndrome: a complex disorder with simple roots.

RettBASE: Rett syndrome database update.

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reactome:R-HSA-9005891

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biological pathway

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Pervasive developmental disorders

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R-HSA-9005891

http://www.w3.org/2001/XMLSchema#string

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Loss of MECP2 binding ability to the NCoR/SMRT complex

Loss of phosphorylation of MECP2 at T308

Loss of MECP2 binding ability to 5hmC-DNA

Loss of MECP2 binding ability to 5mC-DNA

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