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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 HG1497_PATCH: 153,190,041-153,266,223 reverse strand.

GRCh37:JH159150.3

View this gene on the primary assembly.

About this gene

This gene has 11 transcripts (splice variants), 1 gene allele and is associated with 14 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000598049.1MECP2-0021685498aaENSP00000472559.1
 
Protein coding
P51608 -Ensembl CanonicalGENCODE basic
ENST00000601699.1MECP2-00110505486aaENSP00000470011.1
 
Protein coding
C9JH89 D3YJ43 P51608
-GENCODE basic
ENST00000593590.1MECP2-005892172aaENSP00000471217.1
 
Protein coding
B5MCB4 C9JH89 -GENCODE basic
ENST00000601709.1MECP2-00841450aaENSP00000469487.1
 
Protein coding
C9JH89 -CDS 3' incomplete
ENST00000594113.1MECP2-00378434aaENSP00000472083.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000598211.1MECP2-0121299No protein-
 
Processed transcript
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ENST00000600915.2MECP2-0101200No protein-
 
Processed transcript
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ENST00000595642.1MECP2-0111089No protein-
 
Processed transcript
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ENST00000599886.1MECP2-004875No protein-
 
Processed transcript
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ENST00000597080.1MECP2-013436No protein-
 
Processed transcript
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ENST00000595070.1MECP2-006351No protein-
 
Processed transcript
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