Genopathy
Gene-Disorder Association · Article
Gene
MECP2
Methyl-CpG Binding Protein 2
Disorder
Non-Syndromic X-Linked Intellectual Disability
First reported 1977
Supporting publications 6
Key publication · disorder Familial X-linked mental retardation with an X chromosome abnormality.Journal of medical genetics · 1977
Manually curated
Association Review

In brief

The association between MECP2 (Methyl-CpG Binding Protein 2) and Non-Syndromic X-Linked Intellectual Disability is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording pathogenic variants and a causative germline mutation.

Sources 3
Clinical variants 0
Symptoms 0
Compounds 0
Trials 0
Publications 6
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

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02
Provenance

Evidence and sources

3 sources

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

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03
MECP2

The gene

1 source summary

A gene summary alongside the source descriptions it was distilled from.

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04
Non-Syndromic X-Linked Intellectual Disability

The disorder

9 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

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05
Literature

Reading

6 publications

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

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06
Provenance

References & sources

11 references

Every source and publication cited across this dossier, as one numbered reference list.

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