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.
Transcripts
Transcript ID | Name | bp | Protein | Translation ID | Biotype | CCDS | UniProt Match | RefSeq | Flags |
---|---|---|---|---|---|---|---|---|---|
ENST00000303391.6 | MECP2-001 | 10505 | 486aa | ENSP00000301948.6 | Protein coding | CCDS14741 | C9JH89 D3YJ43 P51608 | NM_004992.3 | GENCODE basic, |
ENST00000453960.2 | MECP2-002 | 1685 | 498aa | ENSP00000395535.2 | Protein coding | CCDS48193 | P51608 | NM_001110792.1 | GENCODE basic, |
ENST00000407218.1 | MECP2-005 | 892 | 172aa | ENSP00000384865.1 | Protein coding | B5MCB4 C9JH89 | - | GENCODE basic, | |
ENST00000415944.1 | MECP2-008 | 414 | 50aa | ENSP00000416267.1 | Protein coding | C9JH89 | - | CDS 3' incomplete, | |
ENST00000369957.3 | MECP2-003 | 784 | 34aa | ENSP00000358973.3 | Nonsense mediated decay | - | - | CDS 5' incomplete, | |
ENST00000460227.1 | MECP2-012 | 1299 | No protein | - | Processed transcript | - | - | - | |
ENST00000488293.2 | MECP2-010 | 1200 | No protein | - | Processed transcript | - | - | - | |
ENST00000463644.1 | MECP2-011 | 1089 | No protein | - | Processed transcript | - | - | - | |
ENST00000486506.1 | MECP2-004 | 875 | No protein | - | Processed transcript | - | - | - | |
ENST00000481807.1 | MECP2-013 | 436 | No protein | - | Processed transcript | - | - | - | |
ENST00000496908.1 | MECP2-006 | 351 | No protein | - | Processed transcript | - | - | - |