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Rr27tm2Rohl
Targeted Allele Detail
Summary
Symbol: Rr27tm2Rohl
Name: regulatory region 27; targeted mutation 2, Rolf Ohlsson
MGI ID: MGI:3045724
Synonyms: H19tm2Rohl
Gene: Rr27  Location: unknown  Genetic Position: Chr7, Syntenic
Alliance: Rr27tm2Rohl page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:89915
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Targeted (Modified regulatory region)
Mutations:    Insertion, Nucleotide substitutions
 
Mutation detailsCTCF target site 4 within the imprinting control region (ICR) was modified from a central GTGG motif to ATAT via homologous recombination. A floxed neomycin resistance gene cassette that was included in the targeting vector was excised via in vivo cre-mediated recombination in the germ line. Southern blot analysis and sequence analysis confirmed recombination. (J:89915)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Rr27 Mutation:  6 strains or lines available
References
Original:  J:89915 Pant V, et al., Mutation of a single CTCF target site within the H19 imprinting control region leads to loss of Igf2 imprinting and complex patterns of de novo methylation upon maternal inheritance. Mol Cell Biol. 2004 Apr;24(8):3497-504
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory