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| Nomenclature |
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Symbol:
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Kcnq1tm1Apf
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Name:
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potassium voltage-gated channel, subfamily Q, member 1;
targeted mutation 1, Andrew P Feinberg
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MGI ID: |
MGI:1931858 |
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Synonyms: |
Kvlqt1- |
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Gene:
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Kcnq1
Location:
Chr7:143107254-143427042 bp, + strand
Genetic Position: Chr7,
88.12 cM
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Cochlear abnormalities in Kcnq1tm1Apf/Kcnq1tm1Apf mice
Show the 3 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:66428
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Parent Cell Line:
| E14 (ES Cell) |
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Strain of Origin:
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129P2/OlaHsd
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Mutation description |
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Allele
Type: | |
Targeted (knock-out) |
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Mutation: | |
Insertion |
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Mutation details: Insertion of a neomycin resistance cassette into exon 1 disrupted the gene. The authors predict that all isoforms of the protein would be inactivated in homozygous mutant animals. RT-PCR did not detect expression of the tanscript in tissues of homozygous mice. (J:66428)
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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 Kcnq1 Mutation:
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11 strains or lines available |
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| References |
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Original: |
J:66428
Lee MP et al.,
"Targeted disruption of the kvlqt1 gene causes deafness and gastric hyperplasia in mice"
J Clin Invest 2000 Dec;106(12):1447-55
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All: |
3 reference(s)
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