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| Nomenclature |
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Symbol:
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Rettm2(RET)Jmi
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Name:
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ret proto-oncogene;
targeted mutation 2, Jeffrey Milbrandt
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MGI ID: |
MGI:3057332 |
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Synonyms: |
Ret9, RetRET9 |
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Gene:
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Ret
Location:
Chr6:118151748-118197744 bp, - strand
Genetic Position: Chr6,
55.86 cM, cytoband E3-F1
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Mutation origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:93262
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Parent Cell Line:
| Not Specified (ES Cell) |
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Strain of Origin:
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Not Specified
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Mutation description |
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Allele
Type: | |
Targeted (knock-in) |
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Mutation: | |
Insertion |
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Mutation details: Human RET9 cDNA and a floxed neo were inserted into exon 1 of the endogenous locus. Mating with mice expressing Cre in the germline excised the neo. RT-PCR showed expression of the mutant allele in brain. (J:93262)
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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 Ret Mutation:
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15 strains or lines available |
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| References |
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Original: |
J:93262
Jain S et al.,
"Mice expressing a dominant-negative Ret mutation phenocopy human Hirschsprung disease and delineate a direct role of Ret in spermatogenesis."
Development 2004 Dec;131(21):5503-13
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All: |
8 reference(s)
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