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Allele : Rr27<tm1Rohl> regulatory region 27; targeted mutation 1, Rolf Ohlsson

Primary Identifier  MGI:2653959 Allele Type  Targeted
Attribute String  Modified regulatory region, Null/knockout Gene  Rr27
Transmission  Germline Strain of Origin  (129X1/SvJ x 129S1/Sv)F1-Kitl<+>
Is Recombinase  false Is Wild Type  false
description  Disruption of the Ctcf target sites within the imprinting control region results in a loss of Ifg2 and H19 imprinting when the mutant allele is passaged through the female germline. The loss of imprinting is associated with an 11% increase in neonatal body weight.
molecularNote  The first, third, and fourth Ctcf target sites within the imprinting control region (ICR) were modified from GTGG to ATAT via site directed mutagenesis. A floxed neomycin resistance gene cassette that was included in the targeting vector for selection was excised via in vivo cre-mediated recombination in the germline.
  • mutations:
  • Nucleotide substitutions
  • synonyms:
  • H19<tm1Rohl>,
  • H19<tm1Rohl>
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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

8 Publication categories

Trail: Allele