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Allele : Ppm1d<tm2.1Ble> protein phosphatase 1D magnesium-dependent, delta isoform; targeted mutation 2.1, Benjamin Ebert

Primary Identifier  MGI:7461273 Allele Type  Targeted
Attribute String  Conditional ready Gene  Ppm1d
Transmission  Germline Strain of Origin  C57BL/6J x 129S6/SvEvTac
Is Recombinase  false Is Wild Type  false
molecularNote  A loxP site was inserted into intron 5 and a second loxP site, three copies of SV40 poly(A) signal sequences, an FRT site flanked neomycin resistance gene cassette, followed by a third loxP site, the 3' end of intron 5 and a modified copy of exon 6 were inserted into the 3' UTR of the endogenous exon 6. The modification involves changing threonine codon 476 (ACT) to a stop codon (TGA) (p.T476*) and inserting sequence TTAATTAA downstream for stop codons in the other two reading frames. The neo cassette was removed through subsequent Flp-mediated recombination. Cre recombinase-mediated excision of the floxed endogenous exon 6 enables expression of the modified exon that is analogous to the somatic modifications commonly observed in humans.
  • mutations:
  • Insertion
  • synonyms:
  • Ppm1d<T476*-fl>,
  • Ppm1d<T476-fl>,
  • Ppm1d<T476*-fl>,
  • Ppm1d<T476-fl>
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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

3 Publication categories

Trail: Allele