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| Nomenclature |
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Symbol:
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Admtm1Unc
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Name:
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adrenomedullin;
targeted mutation 1, University of North Carolina
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MGI ID: |
MGI:2176598 |
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Synonyms: |
AM- |
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Gene:
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Adm
Location:
Chr7:110627669-110629819 bp, + strand
Genetic Position: Chr7,
57.7 cM
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Massive generalized edema of Admtm1Unc/Admtm1Unc embryos
Show the 5 image(s) involving this allele.
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Mutation origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:67044
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Parent Cell Line:
| TC1/TC-1 (ES Cell) |
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Strain of Origin:
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129S6/SvEvTac
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Mutation description |
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Allele
Type: | |
Targeted (Reporter) |
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Mutations: | |
Insertion, Intragenic deletion |
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Mutation details: An in-frame EGFP gene and a neomycin resistance cassette were inserted into exon 2, and a genomic fragment corresponding to exons 3 and 4 was deleted. RT-PCR analysis on embryonic RNA of homozygotes demonstrated that no detectable Adm transcript was expressed from this allele. (J:67044)
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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 Adm Mutation:
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1 strain or line available |
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| References |
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Original: |
J:67044
Caron KM et al.,
"Extreme hydrops fetalis and cardiovascular abnormalities in mice lacking a functional Adrenomedullin gene."
Proc Natl Acad Sci U S A 2001 Jan 16;98(2):615-9
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All: |
6 reference(s)
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