Methyl-CpG binding protein 2

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Methyl-CpG binding protein 2 or MECP2 is a gene.[1]

Function[edit | edit source]

MECP2 is a methylation gene and MECP2 mutations are associated with Rett Syndrome, the main cause of intellectual disability in females, and with severe neonatal encephalopathy. MECP2 has a role in RNA binding and chromatin binding. MBA4 is a related gene.[1]

ME/CFS[edit | edit source]

See also[edit | edit source]

Learn more[edit | edit source]

References[edit | edit source]

  1. 1.01.1 "MECP2 - Methyl-CpG binding protein 2 - Gene card". Gene cards. Retrieved May 25, 2022.

The information provided at this site is not intended to diagnose or treat any illness.
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history.