Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 4204
  • Symbol: MECP2
  • Description: methyl-CpG binding protein 2

Marrvel Logo and Link

Export (tab separated) Export to Excel

Disease_Term Source Rank Other Values
Rett syndrome, preserved speech variant, 312750 (3) OMIM high
  • Genome region : Xq28
  • OMIM_ID : 300005 OMIM gene ID
  • OMIM_ID : 312750 OMIM phenotype ID
{Autism susceptibility, X-linked 3}, 300496 (3) OMIM high
  • Genome region : Xq28
  • OMIM_ID : 300005 OMIM gene ID
  • OMIM_ID : 300496 OMIM phenotype ID
Encephalopathy, neonatal severe, 300673 (3) OMIM high
  • Genome region : Xq28
  • OMIM_ID : 300005 OMIM gene ID
  • OMIM_ID : 300673 OMIM phenotype ID
Rett syndrome, 312750 (3) OMIM high
  • Genome region : Xq28
  • OMIM_ID : 300005 OMIM gene ID
  • OMIM_ID : 312750 OMIM phenotype ID
Mental retardation, X-linked syndromic, Lubs type, 300260 (3) OMIM high
  • Genome region : Xq28
  • OMIM_ID : 300005 OMIM gene ID
  • OMIM_ID : 300260 OMIM phenotype ID
Rett syndrome, atypical, 312750 (3) OMIM high
  • Genome region : Xq28
  • OMIM_ID : 300005 OMIM gene ID
  • OMIM_ID : 312750 OMIM phenotype ID
Mental retardation, X-linked, syndromic 13, 300055 (3) OMIM high
  • Genome region : Xq28
  • OMIM_ID : 300005 OMIM gene ID
  • OMIM_ID : 300055 OMIM phenotype ID
Red blood cell traits GWAS high
Schizophrenia GWAS high
Systemic lupus erythematosus GWAS high