Human (GRCh37.p13)
Description

methyl CpG binding protein 2 (Rett syndrome) [Source:HGNC Symbol;Acc:6990]

Gene Synonyms

AUTSX3, MRX16, MRX79, MRXS13, MRXSL, PPMX, RS, RTS, RTT

Location

Chromosome X: 153,287,024-153,363,212 reverse strand.

GRCh37:CM000685.1

View alleles of this gene on alternative sequences

About this gene

This gene has 11 transcripts (splice variants), 1 gene allele, 1 paralogue and is associated with 22 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000303391.6MECP2-00110505486aaENSP00000301948.6
 
Protein coding
CCDS14741C9JH89 D3YJ43 P51608
NM_004992.3GENCODE basic
ENST00000453960.2MECP2-0021685498aaENSP00000395535.2
 
Protein coding
CCDS48193P51608 NM_001110792.1GENCODE basic
ENST00000407218.1MECP2-005892172aaENSP00000384865.1
 
Protein coding
B5MCB4 C9JH89 -GENCODE basic
ENST00000415944.1MECP2-00841450aaENSP00000416267.1
 
Protein coding
C9JH89 -CDS 3' incomplete
ENST00000369957.3MECP2-00378434aaENSP00000358973.3
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000460227.1MECP2-0121299No protein-
 
Processed transcript
---
ENST00000488293.2MECP2-0101200No protein-
 
Processed transcript
---
ENST00000463644.1MECP2-0111089No protein-
 
Processed transcript
---
ENST00000486506.1MECP2-004875No protein-
 
Processed transcript
---
ENST00000481807.1MECP2-013436No protein-
 
Processed transcript
---
ENST00000496908.1MECP2-006351No protein-
 
Processed transcript
---