Rr27tm1.1Ricc
Targeted Allele Detail
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| Symbol: |
Rr27tm1.1Ricc |
| Name: |
regulatory region 27; targeted mutation 1.1, Andrea Riccio |
| MGI ID: |
MGI:6780029 |
| Synonyms: |
hIC1delta1.8 |
| Gene: |
Rr27 Location: Chr7:142133885-142136283 bp Genetic Position: Chr7, Syntenic
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| Alliance: |
Rr27tm1.1Ricc page
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| Germline Transmission: |
Earliest citation of germline transmission:
J:308687
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| Parent Cell Line: |
E14 (ES Cell)
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| Strain of Origin: |
129P2/OlaHsd
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| Allele Type: |
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Targeted (Modified regulatory region) |
| Mutations: |
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Insertion, Intragenic deletion
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Mutation details: The targeting construct replaced the endogenous imprinting control region (ICR) with a mutant corresponding human sequence that deletes a 1.8 kb region found in a familial case of Beckwith-Wiedemann syndrome. Cre-mediated recombination removed a floxed neomycin resistance cassette inserted downstream of the human sequence.
(J:308687)
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| 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
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| Carrying any Rr27 Mutation: |
7 strains or lines available
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| Original: |
J:308687 Freschi A, et al., The number of the CTCF binding sites of the H19/IGF2:IG-DMR correlates with DNA methylation and expression imprinting in a humanized mouse model. Hum Mol Genet. 2021 Jul 28;30(16):1509-1520 |
| All: |
1 reference(s) |
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