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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Bcl2tm1Tsu
targeted mutation 1, Yoshihide Tsujimoto
MGI:2158305
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Bcl2tm1Tsu/Bcl2tm1Tsu involves: 129P2/OlaHsd * ICR MGI:3692763


Genotype
MGI:3692763
hm1
Allelic
Composition
Bcl2tm1Tsu/Bcl2tm1Tsu
Genetic
Background
involves: 129P2/OlaHsd * ICR
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bcl2tm1Tsu mutation (1 available); any Bcl2 mutation (41 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• about 20% survive for 5-7 weeks and the rest (about 10%) live longer than 10 weeks of age
• about 70% die at 2-3 weeks, just before weaning

growth/size/body
• seen in most mutants
• develop polycystic kidney disease, although severity and age of onset varies
• at about 10 days after birth, some mutants are already smaller
• at about 10 days after birth, some mutants are already smaller

hearing/vestibular/ear
• seen in most mutants

hematopoietic system
• small due to accelerated apoptosis of lymphocytes
• exhibit accelerated apoptosis of lymphocytes
• lymphocyte development initially appears normal, however lymphocytes from spleen or thymus lose the differentiated B220+/IgM+ B cell or CD4+/CD8+ T cell subpopulation, respectively
• small due to accelerated apoptosis of lymphocytes
• thymocytes show accelerated cell death in vitro

digestive/alimentary system
• retarded development and accelerated exfoliation of epithelial cells and very few mitotic progenitor cells in the small intestine
• the intestinal lumen shows clusters of apoptotic cells; apoptosis of epithelial cells is not restricted to the villus tip
• the number of mitoses in crypts of small intestine varies considerably, but is smaller than in wild-type
• villi of the small intestine are bizarre in shape
• villi of the small intestine are shorter

renal/urinary system
• kidney architecture is very distored, suggesting that renal failure may be one cause of death
• develop polycystic kidney disease, although severity and age of onset varies
• only few recognizable glomeruli are seen
• dilation of both distal and proximal convoluted tubules due to multiple cysts
• dilation of both distal and proximal convoluted tubules due to multiple cysts
• kidneys are pale

pigmentation
• exhibit a lack of melanin in white hair
• hair hypopigmentation (hair turns white) in the second hair follicle cycle
• hypopigmentation begins at the chin and proceeds to the hip

endocrine/exocrine glands
• the number of mitoses in crypts of small intestine varies considerably, but is smaller than in wild-type
• small due to accelerated apoptosis of lymphocytes

immune system
• small due to accelerated apoptosis of lymphocytes
• exhibit accelerated apoptosis of lymphocytes
• lymphocyte development initially appears normal, however lymphocytes from spleen or thymus lose the differentiated B220+/IgM+ B cell or CD4+/CD8+ T cell subpopulation, respectively
• small due to accelerated apoptosis of lymphocytes
• thymocytes show accelerated cell death in vitro

craniofacial
• seen in most mutants

integument
• exhibit a lack of melanin in white hair





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
05/07/2024
MGI 6.23
The Jackson Laboratory