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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Bbc3tm1Gpz
targeted mutation 1, Gerard P Zambetti
MGI:3692386
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Bbc3tm1Gpz/Bbc3tm1Gpz involves: 129P2/OlaHsd MGI:3697065
cx2
Bbc3tm1Gpz/Bbc3tm1Gpz
Bnip3ltm1Ney/Bnip3ltm1Ney
involves: 129P2/OlaHsd MGI:3819937
cx3
Bbc3tm1Gpz/Bbc3tm1Gpz
Trp53tm1Brd/Trp53tm8Xu
involves: 129P2/OlaHsd * 129S7/SvEvBrd MGI:4946296


Genotype
MGI:3697065
hm1
Allelic
Composition
Bbc3tm1Gpz/Bbc3tm1Gpz
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bbc3tm1Gpz mutation (0 available); any Bbc3 mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• maximum rate of left ventricular pressure rise and fall (dP/dtmax and dP/dtmin, respectively) recover to 77 and 67% of baseline compared to 11 and 11% of baseline in wild-type after 20 minutes of ischemia and 120 minutes of reperfusion
• after 20 minutes of ischemia, followed by 120 minutes of reperfusion, mutant hearts attain 73% of baseline LVDP value, compared to 15% of baseline in wild-type hearts
• upon ischemia/reperfusion, over 50% of the myocardium becomes infarcted in wild-type, compared to only about 25% in mutant hearts

cellular
• cultured thymocytes treated with dexamethazsone are refractory to apoptosis compared to wild-type or Trp53-deficient cells but undergo cell death by 46 hours
• cultured thymocytes maintain viability after gamma-irradiation
• P5 mice exposed to 18 Gy gamma-irradiation show almost complete abrogation of apoptosis when examined after 6 hour recovery
• cell death throughout developing nervous system (EGL, dentate gyrus, retina and subventricular zone of lateral ventricle) of mutants is nearly absent compared to high levels in controls after gamma-irradiation
• apoptosis after ischemia/reperfusion is ~0.3%, compared to ~1% in wild-type, whereas normoxic control hearts show about 0.1% apoptosis

nervous system
• cell death throughout developing nervous system (EGL, dentate gyrus, retina and subventricular zone of lateral ventricle) of mutants is nearly absent compared to high levels in controls after gamma-irradiation

homeostasis/metabolism
• upon ischemia/reperfusion, over 50% of the myocardium becomes infarcted in wild-type, compared to only about 25% in mutant hearts
• after ischemia/reperfusion, LDH release into cardiac effluent is reduced ~50% compared to controls

hematopoietic system
N
• unlike in Bnip3ltm1Ney homozygotes, reticulocytes clearance of mitochondria is normal




Genotype
MGI:3819937
cx2
Allelic
Composition
Bbc3tm1Gpz/Bbc3tm1Gpz
Bnip3ltm1Ney/Bnip3ltm1Ney
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bbc3tm1Gpz mutation (0 available); any Bbc3 mutation (18 available)
Bnip3ltm1Ney mutation (0 available); any Bnip3l mutation (41 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• half of circulating erythrocytes contain mitochondria unlike in wild-type erythrocytes but similar to in Bnip3ltm1Ney homozygotes




Genotype
MGI:4946296
cx3
Allelic
Composition
Bbc3tm1Gpz/Bbc3tm1Gpz
Trp53tm1Brd/Trp53tm8Xu
Genetic
Background
involves: 129P2/OlaHsd * 129S7/SvEvBrd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bbc3tm1Gpz mutation (0 available); any Bbc3 mutation (18 available)
Trp53tm1Brd mutation (5 available); any Trp53 mutation (232 available)
Trp53tm8Xu mutation (0 available); any Trp53 mutation (232 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• the segmental progeria phenotypes observed in Trp53tm1Brd/Trp53tm8Xu mice are rescued
• mice survive longer than Trp53tm1Brd/Trp53tm8Xu mice

reproductive system
N
• testes atrophy observed in Trp53tm1Brd/Trp53tm8Xu mice is rescued
• depletion of adult stem cells in the testes observed in Trp53tm1Brd/Trp53tm8Xu mice is rescued

immune system
• not as severe as in Trp53tm1Brd/Trp53tm8Xu mice

nervous system
N
• depletion of adult stem cells in the brain observed in Trp53tm1Brd/Trp53tm8Xu mice is rescued

digestive/alimentary system
N
• apoptosis in the crypt of small intestine observed in Trp53tm1Brd/Trp53tm8Xu mice is rescued

hematopoietic system
N
• depletion of adult stem cells in the bone marrow observed in Trp53tm1Brd/Trp53tm8Xu mice is rescued
• not as severe as in Trp53tm1Brd/Trp53tm8Xu mice

endocrine/exocrine glands
• not as severe as in Trp53tm1Brd/Trp53tm8Xu mice





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory