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

About this transcript

This transcript has 3 exons, is annotated with 15 domains and features, is associated with 23692 variant alleles and maps to 306 oligo probes.

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
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ENST00000488293.2MECP2-0101200No protein-
 
Processed transcript
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ENST00000463644.1MECP2-0111089No protein-
 
Processed transcript
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ENST00000486506.1MECP2-004875No protein-
 
Processed transcript
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ENST00000481807.1MECP2-013436No protein-
 
Processed transcript
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ENST00000496908.1MECP2-006351No protein-
 
Processed transcript
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Statistics

Exons: 3, Coding exons: 3, Transcript length: 1,685 bps, Translation length: 498 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: P51608

CCDS

This transcript is a member of the Human CCDS set: CCDS48193

Version

ENST00000453960.2

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Transcript having exact match between ENSEMBL and HAVANA:
OTTHUMT00000061145 (version 2)
GENCODE basic gene

This transcript is a member of the Gencode basic gene set.