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Allele : Mecp2<tm1.1Gman> methyl CpG binding protein 2; targeted mutation 1.1, Gail Mandel

Primary Identifier  MGI:6196027 Allele Type  Targeted
Attribute String  Humanized sequence Gene  Mecp2
Transmission  Germline Strain of Origin  C57BL/6NTac
Is Recombinase  false Is Wild Type  false
molecularNote  Exon 3 was targeted with a G>A mutation changing codon 106 from arginine to glutamine (p.Arg106Gln or p.R106Q) in the DNA-binding domain of the encoded peptide. An FRT site flanked neomycin resistance gene cassette that was inserted into intron 3 was subsequently removed through flp-mediated recombination. This allele mimics a human mutation associated with Rett syndrome.
  • mutations:
  • Single point mutation
  • synonyms:
  • Mecp2<317G-to-A>,
  • Mecp2<R106Q>,
  • Mecp2<R106Q>,
  • Mecp2<317G-to-A>
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

4 Publication categories

Trail: Allele