MECP2 (methyl-CpG binding protein 2)

2003-02-01  

Identity

HGNC
LOCATION
Xq28
LOCUSID
ALIAS
AUTSX3,MRX16,MRX79,MRXS13,MRXSL,PPMX,RS,RTS,RTT
FUSION GENES

Other Information

Locus ID:

NCBI: 4204
MIM: 300005
HGNC: 6990
Ensembl: ENSG00000169057

Variants:

dbSNP: 4204
ClinVar: 4204
TCGA: ENSG00000169057
COSMIC: MECP2

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000169057ENST00000303391P51608
ENSG00000169057ENST00000303391D3YJ43
ENSG00000169057ENST00000369957H7BY72
ENSG00000169057ENST00000407218B5MCB4
ENSG00000169057ENST00000415944C9JH89
ENSG00000169057ENST00000453960P51608
ENSG00000169057ENST00000453960A0A140VKC4
ENSG00000169057ENST00000611468A0A087WVW7
ENSG00000169057ENST00000622433A0A087X1U4
ENSG00000169057ENST00000628176A0A0D9SFX7
ENSG00000169057ENST00000630151A0A0D9SEX1
ENSG00000169057ENST00000637917A0A1B0GTV0
ENSG00000169057ENST00000640414I6LM39

Expression (GTEx)

0
5
10
15
20
25
30
35
40

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
381101112024A proteomic approach to investigate the role of the MECP2 gene mutation in Rett syndrome redox regulatory pathways.0
383739422024Genetic analysis of a pedigree with MECP2 duplication syndrome in China.0
384480192024[Genetic analysis and prenatal diagnosis for a Chinese pedigree affected with co-morbid Ornithine carbamoyl transferase deficiency and MECP2 duplication syndrome].0
385784572024CRL4(DCAF13) E3 ubiquitin ligase targets MeCP2 for degradation to prevent DNA hypermethylation and ensure normal transcription in growing oocytes.0
386971122024MECP2 directly interacts with RNA polymerase II to modulate transcription in human neurons.0
387048632024Methyl-CpG-binding protein 2 regulates CYP27A1-induced myometrial contraction during preterm labor.0
381101112024A proteomic approach to investigate the role of the MECP2 gene mutation in Rett syndrome redox regulatory pathways.0
383739422024Genetic analysis of a pedigree with MECP2 duplication syndrome in China.0
384480192024[Genetic analysis and prenatal diagnosis for a Chinese pedigree affected with co-morbid Ornithine carbamoyl transferase deficiency and MECP2 duplication syndrome].0
385784572024CRL4(DCAF13) E3 ubiquitin ligase targets MeCP2 for degradation to prevent DNA hypermethylation and ensure normal transcription in growing oocytes.0
386971122024MECP2 directly interacts with RNA polymerase II to modulate transcription in human neurons.0
387048632024Methyl-CpG-binding protein 2 regulates CYP27A1-induced myometrial contraction during preterm labor.0
366403272023Mutations in the transcriptional regulator MeCP2 severely impact key cellular and molecular signatures of human astrocytes during maturation.7
367245572023Human MECP2 transgenic rats show increased anxiety, severe social deficits, and abnormal prefrontal neural oscillation stability.3
368271842023DDX47, MeCP2, and other functionally heterogeneous factors protect cells from harmful R loops.7

Citation

Dessen P

MECP2 (methyl-CpG binding protein 2)

Atlas Genet Cytogenet Oncol Haematol. 2003-02-01

Online version: http://atlasgeneticsoncology.org/gene/41330/css/lib/gene-explorer/js/lib/jquery-3.5.1.min.js