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Loss of Function of MECP2 in Rett Syndrome
Instance of the biological pathway in Homo sapiens with Reactome ID (R-HSA-9005891).
Statements about
Loss of Function of MECP2 in Rett Syndrome
Exact Match
https://identifiers.org/reactome:R-H ...
Instance Of
Biological Pathway
Part Of
Has Part(s)
Loss of Phosphorylation of MECP2 at T308
Pervasive Developmental Disorders
Loss of MECP2 Binding Ability to the NCoR/SMRT Complex
Loss of MECP2 Binding Ability to 5mC-DNA
Loss of MECP2 Binding Ability to 5hmC-DNA
