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Gene ENSMUSG00000031393 (Mecp2)
Chromosomal location
Chr X: 71272167 - 71330975 (-)
Description
methyl CpG binding protein 2 Gene [Source:MGI (curated);Acc:Mecp2-002]
RefSeq_dna
NM_010788 NM_001081979 
RefSeq_peptide
NP_034918.1 NP_001075448.1 
UniGene
Mm.131408 
MGI
MGI:99918 
Uniprot/SWISSPROT
Q9Z2D6 
Uniprot/SPTREMBL
B1AUZ2 B1AUZ3 
Human Ortholog
ENSG00000169057 (MECP2)
Omim 105830 - ANGELMAN SYNDROME  300055 - MENTAL RETARDATION, X-LINKED, SYNDROMIC 13  300260 - LUBS X-LINKED MENTAL RETARDATION SYNDROME  300496 - AUTISM, X-LINKED, SUSCEPTIBILITY TO, 3  300673 - ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS  312750 - RETT SYNDROME  
UniTrap UNI3053
Vector Insertion
Chr X: 71330848 - 71330933
Public Clones BC0189 (sanger)
Private Clones not available
Severity of mutation (?) Insertion after 0% of polypeptide chain
Proposed experimental design for vector insertion validation (?)

UniTrap UNI21035
Vector Insertion
Chr X: 71325372 - 71330848
Public Clones (sanger)
Private Clones OST345175 (lexicon)
Severity of mutation (?) Insertion after 0% of polypeptide chain
Proposed experimental design for vector insertion validation (?)

UniTrap UNI11929
Vector Insertion
Chr X: 71282672 - 71325247
Public Clones (sanger) Q011C08 (ggtc)
Private Clones not available
Severity of mutation (?) Insertion after 2% of polypeptide chain
Proposed experimental design for vector insertion validation (?)

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