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Allele : Vsx2<tm1.1Eml> visual system homeobox 2; targeted mutation 1.1, Edward M Levine

Primary Identifier  MGI:5449356 Allele Type  Targeted
Attribute String  Not Specified Gene  Vsx2
Transmission  Germline Strain of Origin  (129X1/SvJ x 129S1/Sv)F1-Kitl<+>
Is Recombinase  false Is Wild Type  false
molecularNote  A self excising selection cassette (ACN) was inserted in intron 3 and the bases agg were changed to tgg in exon 4 via homologous recombination. The base changes result in an arginine to tryptophan substitution at position 227 (R227W). Cre mediated recombination in the male germ line removed the selection cassette. Protein expression is similar to wild-type protein but DNA binding is reduced.
  • mutations:
  • Insertion,
  • Nucleotide substitutions
  • synonyms:
  • Vsx2<R227W>,
  • R227W,
  • Vsx2<R227W>,
  • R227W
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

4 Publication categories