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Allele : Tg(hs636-cre/ERT2,-GFP)266Jlr transgene insertion 266, John Rubenstein

Primary Identifier  MGI:6160933 Allele Type  Transgenic
Attribute String  Inducible, Recombinase, Reporter Gene  Tg(hs636-cre/ERT2,-GFP)266Jlr
Strain of Origin  FVB/NJ Induced With  tamoxifen
Is Recombinase  true Is Wild Type  false
molecularNote  This transgene contains the human enhancer element hs636 -- which resides on human Chr 3 within the arginine and serine rich coiled-coil 1 (RSRC1) locus -- followed by a mouse minimal Hsp68 promoter, the cre/ERT2 fusion gene, an internal ribosomal entry site (IRES), and a green fluorescent protein reporter gene. The fusion gene encodes Cre recombinase joined to a modified ligand-binding domain of the human estrogen receptor that preferentially binds tamoxifen or 4-hydroxytamoxifen, but not endogenous 17beta-estradiol; upon binding to tamoxifen, the cre/ERT2 protein is translocated to the nucleus.
  • mutations:
  • Insertion
  • synonyms:
  • Tg(RSRC1-cre/ERT2, GFP)266Jlr,
  • Tg(RSRC1-cre/ERT2, GFP)266Jlr,
  • 636-CreER-IRES-GFP,
  • 636-CreER-IRES-GFP
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

Trail: Allele

0 Driven By

2 Publication categories

Trail: Allele