MECP2

methyl-CpG binding protein 2

HCNC Approved Symbol

MECP2 (HGNC:6990)

Genomic Coordinates

23:154,021,573 - 154,097,717 (Xq28)

Synonyms

RTT, MRX16, MRX79

Disease Associations

This gene is associated with the following 7 diseases in OMIM.

View More Disease InfoView Less Disease Info

Disease NameOMIM IDInheritance

{Autism susceptibility, X-linked 3}

300496XL

Encephalopathy, neonatal severe

300673X-linked recessive

Intellectual developmental disorder, X-linked syndromic 13

300055X-linked recessive

Intellectual developmental disorder, X-linked syndromic, Lubs type

300260X-linked recessive

Rett syndrome

312750X-linked dominant

Rett syndrome, atypical

312750X-linked dominant

Rett syndrome, preserved speech variant

312750X-linked dominant