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Cftrtm1.1Sdw
Targeted Allele Detail
Summary
Symbol: Cftrtm1.1Sdw
Name: cystic fibrosis transmembrane conductance regulator; targeted mutation 1.1, Steve D Wilton
MGI ID: MGI:7263374
Synonyms: Cftrdelta9
Gene: Cftr  Location: Chr6:18170686-18322767 bp, + strand  Genetic Position: Chr6, 8.1 cM, cytoband A3
Alliance: Cftrtm1.1Sdw page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:323560
Parent Cell Line:  Bruce 4 (ES Cell)
Strain of Origin:  B6.Cg-Thy1a
Mutation
description
Allele Type:    Targeted (Modified isoform(s))
Mutation:    Intragenic deletion
    Exon 9 was flanked with loxP sites. Cre-mediated recombination deleted exon 9 in the germline. (J:323560)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 2 anatomical structure(s)
Find Mice (IMSR)
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
Carrying any Cftr Mutation:  98 strains or lines available
References
Original:  J:323560 Martinovich KM, et al., Investigating the Implications of CFTR Exon Skipping Using a Cftr Exon 9 Deleted Mouse Model. Front Pharmacol. 2022;13:868863
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory