Ildr1tm1Lwa
Targeted Allele Detail
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Symbol: |
Ildr1tm1Lwa |
Name: |
immunoglobulin-like domain containing receptor 1; targeted mutation 1, Lei Wang |
MGI ID: |
MGI:5752278 |
Gene: |
Ildr1 Location: Chr16:36514340-36547166 bp, + strand Genetic Position: Chr16, 25.88 cM
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Alliance: |
Ildr1tm1Lwa page
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Germline Transmission: |
Earliest citation of germline transmission:
J:221594
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Parent Cell Line: |
W4 (ES Cell)
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Strain of Origin: |
129S6/SvEvTac
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Allele Type: |
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Targeted (Conditional ready, Null/knockout, Reporter) |
Mutation: |
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Insertion
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Mutation details: A construct consisting of an FRT site, splice acceptor site, IRES, LacZ gene, loxP site neo cassette, FRT site and loxP site was inserted upstream of exon 2 and a loxP site was inserted downstream of exon 3 via homologous recombination.
(J:221594)
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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 Ildr1 Mutation: |
37 strains or lines available
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Original: |
J:221594 Sang Q, et al., ILDR1 deficiency causes degeneration of cochlear outer hair cells and disrupts the structure of the organ of Corti: a mouse model for human DFNB42. Biol Open. 2015 Mar 27;4(4):411-8 |
All: |
1 reference(s) |
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