MECP2

GENERAL INFORMATION

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Gene name

MECP2

Gene description

Methyl CpG binding protein 2

Protein class

Cancer-related genes
Disease related genes
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

7
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Ubiquitous nuclear expression at variable levels.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 3 antibodies.
HPA000593 , HPA001341 , CAB037264
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

MECP2 (HGNC Symbol)

Synonyms

MRX16, MRX79, RTT

Description

Methyl CpG binding protein 2 (HGNC Symbol)

Entrez gene summary

DNA methylation is the major modification of eukaryotic genomes and plays an essential role in mammalian development. Human proteins MECP2, MBD1, MBD2, MBD3, and MBD4 comprise a family of nuclear proteins related by the presence in each of a methyl-CpG binding domain (MBD). Each of these proteins, with the exception of MBD3, is capable of binding specifically to methylated DNA. MECP2, MBD1 and MBD2 can also repress transcription from methylated gene promoters. In contrast to other MBD family members, MECP2 is X-linked and subject to X inactivation. MECP2 is dispensible in stem cells, but is essential for embryonic development. MECP2 gene mutations are the cause of most cases of Rett syndrome, a progressive neurologic developmental disorder and one of the most common causes of mental retardation in females. [provided by RefSeq, Jul 2009]

Chromosome

X

Cytoband

q28

Chromosome location (bp)

154021573 - 154097755

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000169057 (version 78.38)

Entrez gene

4204

UniProt

P51608 (UniProt - Evidence at protein level)

neXtProt

NX_P51608

Antibodypedia

MECP2 antibodies


PROTEIN BROWSER

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ENST00000303391
 
ENST00000407218
 
ENST00000415944
 
ENST00000453960
 
ENST00000611468
 
ENST00000619732
 
ENST00000622433
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

MECP2-001 ENSP00000301948
ENST00000303391
P51608
Show all »
Show » Show » 486 52.4 No 0
MECP2-002 ENSP00000395535
ENST00000453960
P51608
Show all »
Show » Show » 498 53.3 No 0
MECP2-005 ENSP00000384865
ENST00000407218
B5MCB4
Show all »
Show » Show » 172 19.1 No 0
MECP2-008 ENSP00000416267
ENST00000415944
C9JH89
Show all »
Show » 50 5.7 No 0
MECP2-201 ENSP00000479736
ENST00000611468
D5L9I4
Show all »
Show » Show » 168 18.7 No 0
MECP2-202 ENSP00000480973
ENST00000619732
E9LUH4
Show all »
Show » Show » 509 54.8 No 0
MECP2-203 ENSP00000484470
ENST00000622433
C6KG44
Show all »
Show » Show » 324 34.9 No 0