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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rnpc3tm1c(EUCOMM)Wtsi
targeted mutation 1c, Wellcome Trust Sanger Institute
MGI:6269405
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Ndor1Tg(UBC-cre/ERT2)1Ejb/Ndor1+
Rnpc3tm1c(EUCOMM)Wtsi/Rnpc3+
involves: 129S/SvEv * C57BL/6 * C57BL/6N MGI:6276274
cn2
Ndor1Tg(UBC-cre/ERT2)1Ejb/Ndor1+
Rnpc3tm1c(EUCOMM)Wtsi/Rnpc3tm1c(EUCOMM)Wtsi
involves: 129S/SvEv * C57BL/6 * C57BL/6N MGI:6276277


Genotype
MGI:6276274
cn1
Allelic
Composition
Ndor1Tg(UBC-cre/ERT2)1Ejb/Ndor1+
Rnpc3tm1c(EUCOMM)Wtsi/Rnpc3+
Genetic
Background
involves: 129S/SvEv * C57BL/6 * C57BL/6N
Cell Lines EPD0441_1_B10
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ndor1Tg(UBC-cre/ERT2)1Ejb mutation (6 available); any Ndor1 mutation (32 available)
Rnpc3tm1c(EUCOMM)Wtsi mutation (0 available); any Rnpc3 mutation (41 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• tamoxifen-treated adult mice appear phenotypically normal with no significant weight loss relative to control mice




Genotype
MGI:6276277
cn2
Allelic
Composition
Ndor1Tg(UBC-cre/ERT2)1Ejb/Ndor1+
Rnpc3tm1c(EUCOMM)Wtsi/Rnpc3tm1c(EUCOMM)Wtsi
Genetic
Background
involves: 129S/SvEv * C57BL/6 * C57BL/6N
Cell Lines EPD0441_1_B10
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ndor1Tg(UBC-cre/ERT2)1Ejb mutation (6 available); any Ndor1 mutation (32 available)
Rnpc3tm1c(EUCOMM)Wtsi mutation (0 available); any Rnpc3 mutation (41 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• at 8 days after tamoxifen (TAM) treatment, adult mice show signs of malnutrition and stress (scruffy coat, docile, and hunched behavior) requiring euthanasia

growth/size/body
• adult mice show irreversible weight loss by 6 days after TAM treatment

behavior/neurological
• hunched behavior at 8 days after TAM treatment

immune system
• infiltration of immune cells in small intestinal epithelium at 6 days after TAM treatment
• signs of erosive esophagitis at 8 days after TAM treatment
• significant reduction in thymus weight at 8 days at 8 days after TAM treatment
• significantly smaller thymus with no discernible medullary or cortical regions at 8 days after TAM treatment
• at 8 days after TAM treatment
• at 8 days after TAM treatment
• significant leucopenia at 8 days after TAM treatment
• significant decrease in lymphocyte number at 8 days after TAM treatment
• significant decrease in monocyte number at 8 days after TAM treatment

digestive/alimentary system
• significant increase in the number of apoptotic cells in the highly proliferative, stem/progenitor compartment of the small intestinal crypts at 2 and 4 days after TAM treatment
• reduced cell proliferation in the proliferative compartment of the small intestinal epithelium at 4 days after TAM treatment
• marked reduction in BrdU+ cells in small intestinal crypts at 4 days after TAM treatment
• new BrdU+ crypt-like structures corresponding to sites of regeneration at 6 and 8 days after TAM treatment
• severe atrophy of the entire gastrointestinal epithelium with mucosa disruption from the esophagus to the rectum at 8 days after TAM treatment
• extensive degeneration of the epithelial layer interspersed with discrete pockets of regenerating crypt-like structures
• disrupted organization of the squamous epithelium of the esophagus at 8 days after TAM treatment
• at 8 days after TAM treatment, the epithelial monolayer lining the small intestine and colon contains vacuolated epithelial cells scattered throughout the submucosa; epithelial layer degeneration is intermixed with discrete pockets of regenerating crypt-like structures
• loss of epithelial integrity in the small intestine and colon with nuclei rounding up and cells losing apico-basal polarity at 4 days after TAM treatment
• highly disorganized small intestine epithelium, with crypt loss, decreased villus height, infiltration of immune cells, and ulceration at 6 days after TAM treatment
• thinner and flatter epithelial cells in the colon at 6 days after TAM treatment
• at 8 days after TAM treatment
• loss of crypt structure in the colon at 4 days after TAM treatment
• large vacuolated spaces in colonic crypts at 6 days after TAM treatment
• loss of crypt structure in the small intestine at 4 days after TAM treatment
• reduced villus height in the small intestine at 6 days after TAM treatment
• degeneration of columnar mucous epithelium of the glandular stomach at 8 days after TAM treatment
• infiltration of immune cells in small intestinal epithelium at 6 days after TAM treatment
• signs of erosive esophagitis at 8 days after TAM treatment

hematopoietic system
• significant reduction in thymus weight at 8 days at 8 days after TAM treatment
• significantly smaller thymus with no discernible medullary or cortical regions at 8 days after TAM treatment
• at 8 days after TAM treatment
• at 8 days after TAM treatment
• significant anemia at 8 days after TAM treatment
• significant decrease in RBC number at 8 days after TAM treatment
• severe thrombocytopenia at 8 days after TAM treatment
• significant leucopenia at 8 days after TAM treatment
• significant decrease in lymphocyte number at 8 days after TAM treatment
• significant decrease in monocyte number at 8 days after TAM treatment

integument
• paucity of sebaceous glands at 8 days after TAM treatment
• scruffy coat at 8 days at 8 days after TAM treatment
• mild skin abnormalities at 8 days after TAM treatment
• attenuated epidermis at 8 days after TAM treatment

endocrine/exocrine glands
• loss of crypt structure in the colon at 4 days after TAM treatment
• large vacuolated spaces in colonic crypts at 6 days after TAM treatment
• loss of crypt structure in the small intestine at 4 days after TAM treatment
• significant reduction in thymus weight at 8 days at 8 days after TAM treatment
• significantly smaller thymus with no discernible medullary or cortical regions at 8 days after TAM treatment
• at 8 days after TAM treatment
• at 8 days after TAM treatment
• paucity of sebaceous glands at 8 days after TAM treatment

cellular
• significant increase in the number of apoptotic cells in the highly proliferative, stem/progenitor compartment of the small intestinal crypts at 2 and 4 days after TAM treatment
• reduced cell proliferation in the proliferative compartment of the small intestinal epithelium at 4 days after TAM treatment
• marked reduction in BrdU+ cells in small intestinal crypts at 4 days after TAM treatment
• new BrdU+ crypt-like structures corresponding to sites of regeneration at 6 and 8 days after TAM treatment





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory