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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cftrtm1Cam
targeted mutation 1, University of Cambridge
MGI:1857544
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cftrtm1Cam/Cftrtm1Cam involves: 129S/SvEv MGI:2177436


Genotype
MGI:2177436
hm1
Allelic
Composition
Cftrtm1Cam/Cftrtm1Cam
Genetic
Background
involves: 129S/SvEv
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cftrtm1Cam mutation (1 available); any Cftr mutation (98 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• a few survive up to 45 days (J:23850)
• pups fail to thrive and about 80% die 2-5 days after birth, the rest survive up to 45 days, with a large percentage of survivors dying around 21 days (J:23850)

digestive/alimentary system
• dilation and blockage of pancreatic ducts in 5 of 10 mutants aged 17 days or older
• distension of the intestine in observed proximally to the blockage and within the distended area, the majority of the intestinal villi are severely atrophic and necrotic in places
• crypts of Lieberkuhn are severely dilated with mucus
• cecum is reduced
• crypt distension and mucus hypersecretion in the colon
• crypts of the jejunum and ileum are filled with excessive mucus, indicating gastrointestinal mucus accumulation
• variable penetrance of intestinal obstruction in the jejunum and meconium blockage of ileum (meconium ileus) (J:2584)
• death caused by severe peritonitis

endocrine/exocrine glands
• dilation and blockage of pancreatic ducts in 5 of 10 mutants aged 17 days or older
• crypts of Lieberkuhn are severely dilated with mucus
• acinar dilation although no obvious accumulation of mucus

growth/size/body
• those surviving past 2-5 days of age are runted and half the weight of wild-type

immune system
• death caused by severe peritonitis
• several mutants develop eye infections and are prone to persistent eye closure

vision/eye
• acinar dilation although no obvious accumulation of mucus

respiratory system
N
• no accumulation of mucus in the lungs

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
cystic fibrosis DOID:1485 OMIM:219700
J:2584





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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory