Summary |
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Variant origin |
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Variant description |
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Phenotypes |
View phenotypes and curated references for all genotypes (concatenated display).
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Expression |
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Notes |
Cfld2 exhibits additive inheritance.
Mapping and Phenotype information for this QTL, its variants and associated markersJ:80598216 (C57BL/6J-Cftrtm1Unc x BALB/cJ-Cftrtm1Unc)F2 animals were typed for 114 microsatellite markers at an average spacing of 15 cM to identify QTLs affecting cystic fibrosis-associated lung disease. Parental strain C57BL/6J-Cftrtm1Unc exhibits increased collagen deposition and alveolar interstitial thickening compared to BALB/cJ-Cftrtm1Unc. A QTL named Cfld1 (cystic fibrosis lung disease 1) mapped from 83 cM - 107 cM on mouse Chromosome 2 with a LOD score of 3.0 at D2Mit528 (87.4 cM). Cfld1 is associated with lung fibrosis with BALB/cJ-derived alleles exhibiting recessive inheritance. Cfld2 mapped from 61.5 cM - 74.1 cM on mouse Chromosome 6 with a LOD score of 3.4 at D6Mit198 (67 cM). BALB/cJ-derived alleles confer additively inherited lung fibrosis at Cfld2. Cfld3 mapped from 4.1 cM - 16.4 cM on mouse Chromosome 17 with a LOD score of 3.2 at D17Mit57 (7.6 cM). Cfld3 is associated with lung fibrosis in male animals with C57BL/6J-derived alleles exhibiting additive inheritance. Cfld4 mapped to 50.3 cM - 60 cM on mouse Chromosome 7 with a LOD score of 3.1 at D7Mit238 (53 cM). Cfld4 is associated with alveoli count in female animals with BALB/cJ-derived alleles exhibiting dominant inheritance. |
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References |
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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 |
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