Human (GRCh38.p14)
Description

methyl-CpG binding protein 2 [Source:HGNC Symbol;Acc:HGNC:6990]

Gene Synonyms

MRX16, MRX79, RTT

Location

Chromosome X: 154,021,573-154,137,103 reverse strand.

GRCh38:CM000685.2

About this gene

This gene has 30 transcripts (splice variants), 195 orthologues, 1 paralogue and is associated with 16 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000453960.7MECP2-20510343498aaENSP00000395535.2
 
Protein coding
CCDS48193P51608-2 NM_001110792.2MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicTSL:1
ENST00000303391.11MECP2-20110467486aaENSP00000301948.6
 
Protein coding
CCDS14741P51608-1 NM_004992.4MANE Plus ClinicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000630151.3MECP2-21810452486aaENSP00000486089.2
 
Protein coding
CCDS14741A0A0D9SEX1 D3YJ43 -APPRIS P1TSL:5
ENST00000415944.4MECP2-2041907172aaENSP00000416267.2
 
Protein coding
C9JH89 -GENCODE PrimaryGENCODE BasicTSL:5
ENST00000628176.2MECP2-2161712172aaENSP00000486978.1
 
Protein coding
A0A0D9SFX7 -GENCODE PrimaryGENCODE BasicTSL:3
ENST00000637917.2MECP2-2231298333aaENSP00000489847.2
 
Protein coding
A0A0S2Z401 A0A1B0GTV0 -TSL:5
ENST00000407218.5MECP2-2031174184aaENSP00000384865.2
 
Protein coding
B5MCB4 -GENCODE BasicTSL:5
ENST00000675526.2MECP2-226121261aaENSP00000501710.1
 
Nonsense mediated decay
A0A6Q8PF93 --
ENST00000674996.2MECP2-225112658aaENSP00000502832.1
 
Nonsense mediated decay
A0A6Q8PHQ3 --
ENST00000369957.5MECP2-20278437aaENSP00000358973.4
 
Nonsense mediated decay
H7BY72 -TSL:3
ENST00000713611.1MECP2-23077754aaENSP00000518906.1
 
Nonsense mediated decay
---
ENST00000460227.4MECP2-2061298No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000488293.4MECP2-2101198No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000463644.5MECP2-2071088No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000626422.2MECP2-214835No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000627864.1MECP2-215581No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000631210.1MECP2-219490No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000611468.2MECP2-212366No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000625300.1MECP2-213350No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000496908.5MECP2-211342No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000676382.1MECP2-228313No protein-
 
Protein coding CDS not defined
---
ENST00000700484.1MECP2-229197No protein-
 
Protein coding CDS not defined
---
ENST00000637533.1MECP2-221140No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000637791.1MECP2-222101No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000637467.1MECP2-220101No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000638041.1MECP2-224100No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000486506.5MECP2-2092907No protein-
 
Retained intron
--TSL:5
ENST00000629277.1MECP2-2172558No protein-
 
Retained intron
--TSL:NA
ENST00000675841.1MECP2-2271201No protein-
 
Retained intron
---
ENST00000481807.3MECP2-208436No protein-
 
Retained intron
--TSL:3

Retirement notice

Human only - retirement of this view

As of Ensembl release 93 this view will no longer be available for human, because we feel that the density of known human genetic variation is too great for the display to be informative in its current form.

Other species will not be affected, as they have less variation data.

For more information about the decision and on how to find variation data for a gene, please see our blog post.