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| Nomenclature |
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Symbol:
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H19tm1Tilg
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Name:
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H19 fetal liver mRNA;
targeted mutation 1, Shirley M Tilghman
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MGI ID: |
MGI:1930620 |
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Synonyms: |
deltaH19, H19-, H19delta13 |
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Gene:
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H19
Location:
Chr7:142575529-142578143 bp, - strand
Genetic Position: Chr7,
87.97 cM
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Mutation
origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:25091
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Parent Cell Line:
| CCE/EK.CCE (ES Cell) |
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Strain of Origin:
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129S/SvEv-Gpi1c
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Mutation
description |
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Allele
Type: | |
Targeted (knock-out) |
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Mutations: | |
Insertion, Intragenic deletion |
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Mutation details: A neomycin resistance cassette replaced the entire coding region (3kb) and 10kb of 5' flanking sequence. (J:25091)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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Disease models
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available |
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Carrying any H19 Mutation:
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2 strains or lines available |
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| References |
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Original: |
J:25091
Leighton PA et al.,
"Disruption of imprinting caused by deletion of the H19 gene region in mice [see comments]"
Nature 1995 May 4;375(6526):34-9
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All: |
17 reference(s)
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Analysis Tools
