Cftrtm1Hgu
Targeted Allele Detail
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Symbol: |
Cftrtm1Hgu |
Name: |
cystic fibrosis transmembrane conductance regulator; targeted mutation 1, MRC Human Genetics Unit |
MGI ID: |
MGI:1856710 |
Synonyms: |
cf, cftrm1HGU, Cftrm1Hgu, CftrTgH(neoim)1Hgu, CftrTgH(neoim)Hgu, EDI |
Gene: |
Cftr Location: Chr6:18170686-18322767 bp, + strand Genetic Position: Chr6, 8.1 cM, cytoband A3
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Alliance: |
Cftrtm1Hgu page
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Generation 27 and 28 Cftrtm1Hgu/Cftrtm1Hgu mice exhibit focal hypertrophy of goblet cells
Show the 1 phenotype image(s) involving this allele.
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Germline Transmission: |
Earliest citation of germline transmission:
J:14614
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Parent Cell Line: |
E14 (ES Cell)
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Strain of Origin: |
129P2/OlaHsd
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Allele Type: |
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Targeted (Null/knockout) |
Mutation: |
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Insertion
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Mutation details: An insertion of a vector into intron 9 that included exon 10 interrupted by a neomycin selection gene. RT-PCR analysis on tissues derived from homozygous mice demonstrated that a low level of wild-type transcript was produced from this allele by exon skipping (J:20037).
(J:14614, J:20037)
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View phenotypes and curated references for all genotypes (concatenated display).
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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 Cftr Mutation: |
97 strains or lines available
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Original: |
J:14614 Dorin JR, et al., Cystic fibrosis in the mouse by targeted insertional mutagenesis [see comments]. Nature. 1992 Sep 17;359(6392):211-5 |
All: |
28 reference(s) |
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