KOMP Knock Out Knockout Mouse Mice
Mecp2 methyl CpG binding protein 2 Synonyms: 1500041B07Rik, D630021H01Rik, Mbd5, WBP10 Gene nomenclature, locus information, and GO, OMIM, and PMID associations
are updated daily from MGI
MGI: MGI:99918 ( Current, 37.63cM, Gene) Ensembl: ENSMUSG31393 ( Mecp2) NCBI: 17257, 17654 Vega: OTTMUSG17654 ( Mecp2, methyl CpG binding protein 2) CCDS: 28835.1, 41016, 41017 OMIM:
, ANGELMAN SYNDROME; AS
, METHYL-CpG-BINDING PROTEIN 2; MECP2
, MENTAL RETARDATION, X-LINKED, SYNDROMIC 13; MRXS13
, LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL
, AUTISM, X-LINKED, SUSCEPTIBILITY TO, 3
, ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS
RETT SYNDROME; RTT Gene Ontology: Mecp2
Mouse Phenome DB: Mecp2
UCSC: Chr.X:74,026,821-74,085,636(-) IMPC: Mecp2
Non-KOMP projects associated with this gene exist at: EUCOMM, NORCOMM, TIGM. You can view the status of all IKMC projects for Mecp2. Researchers interested in Mecp2 are also interested* in
* Based on co-mentions in published literature. For more gene-gene associations visit genecloud.org.
The KOMP Repository Collection is located at the MMRRC at the University of California, Davis and Children’s Hospital Oakland Research Institute. Question? Comments? For Mice, Cells, and germplasm please contact us at firstname.lastname@example.org, US 1-888-KOMP-MICE or International +1-530-752-KOMP, or for vectors email@example.com or +1-510-450-7917.