Del(5Gtf2i-Limk1)1Uta
Targeted Allele Detail
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| Nomenclature |
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Symbol:
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Del(5Gtf2i-Limk1)1Uta
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Name:
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deletion, Chr 5, Uta Francke 1
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MGI ID: |
MGI:5317120 |
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Synonyms: |
PD |
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Gene:
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Del(5Gtf2i-Limk1)1Uta
Location:
unknown
Genetic Position: Chr5,
Syntenic
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Mutation
origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:182796
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Parent Cell Line:
| AB2.2 (ES Cell) |
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Strain of Origin:
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129S7/SvEvBrd-Hprtb-m2
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Mutation
description |
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Allele
Type: | |
Targeted (other) |
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Mutation: | |
Intragenic deletion |
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Mutation details: Cre-mediated recombination of ES cells carrying Limk1tm1Uta and Trim50tm1Uta removed all genomic sequence between the two alleles (including Limk1, Eln, Wbscr26, Cldn13, Wbscr27, Cldn4, Cldn3, Abhd11, Stx1a, Wbscr22, Wbscr18, Vps37d, Mlxipl, Tbl2, Bcl7b, Baz1b, Fzd9, Fkbp6 and Trim50). (J:182796)
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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 Del(5Gtf2i-Limk1)1Uta Mutation:
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0 strains or lines available |
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| References |
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Original: |
J:182796
Li HH et al.,
"Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice."
EMBO Mol Med 2009 Apr;1(1):50-65
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All: |
3 reference(s)
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Analysis Tools
