MECP2 gene homepage

MSeqDR-LSDB: Mitochondrial Disease LSDB

General information
Gene symbol	MECP2
Gene name	methyl CpG binding protein 2 (Rett syndrome)
Chromosome	X
Chromosomal band	q28
Imprinted	Unknown
Genomic reference	NC_000023.10
Transcript reference	NM_001110792.1, NM_004992.3, XM_005274681.1, XM_005274682.1, XM_005274683.1
Associated with diseases	-
Citation reference(s)	-
Curators (0)	-
Total number of public variants reported	0
Unique public DNA variants reported	0
Individuals with public variants	0
Hidden variants	0
Download all this gene's data	Download all data
Notes	MSeqDR-LSDB
Date created	November 12, 2013

Links to other resources
HGNC	6990
Entrez Gene	4204
PubMed articles	MECP2
OMIM - Gene	300005
HGMD	MECP2
GeneCards	MECP2
GeneTests	MECP2

Active transcripts

Legend

Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.

ID	Chr	Name	NCBI ID	NCBI Protein ID
00000885	X	transcript variant X2	XM_005274682.1	XP_005274739.1
00000886	X	transcript variant X3	XM_005274683.1	XP_005274740.1
00000887	X	transcript variant X1	XM_005274681.1	XP_005274738.1
00000888	X	transcript variant 1	NM_004992.3	NP_004983.1
00000889	X	transcript variant 2	NM_001110792.1	NP_001104262.1

Copyright & disclaimer
; NuclearMitome http://www.transgenomic.com

Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium

MSeqDR-LSDB Mitochondrial Disease Locus Specific Database

MECP2 (methyl CpG binding protein 2 (Rett syndrome))

MECP2 gene homepage

Active transcripts

Legend