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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Usp22tm1a(KOMP)Wtsi
targeted mutation 1a, Wellcome Trust Sanger Institute
MGI:4364127
Summary 3 genotypes


Genotype
MGI:5631666
hm1
Allelic
Composition
Usp22tm1a(KOMP)Wtsi/Usp22tm1a(KOMP)Wtsi
Genetic
Background
C57BL/6N-Usp22tm1a(KOMP)Wtsi/Wtsi
Cell Lines EPD0119_2_D11
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Usp22tm1a(KOMP)Wtsi mutation (3 available); any Usp22 mutation (33 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging




Genotype
MGI:5796649
hm2
Allelic
Composition
Usp22tm1a(KOMP)Wtsi/Usp22tm1a(KOMP)Wtsi
Genetic
Background
C57BL/6-Usp22tm1a(KOMP)Wtsi
Cell Lines EPD0119_2_D11
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Usp22tm1a(KOMP)Wtsi mutation (3 available); any Usp22 mutation (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• contrary to expectation, homozygotes are born with the expected Mendelian frequency and are viable as adults

growth/size/body
• at 4 months of age, body weight is reduced by 40% relative to controls
• at 4 months of age, mice exhibit growth retardation relative to wild-type and heterozygous controls

digestive/alimentary system
• adult mice exhibit ~50% and ~45% more chromogranin A (CGA)-positive enteroendocrine cells in the crypts and villi of the small intestine, respectively, relative to controls
• adult mice show impaired cell differentiation in the small intestine epithelium
• at 4 months of age, mice show a slight increase in the number of olfactomedin-positive stem cells located near the crypt base of the small intestine relative to controls
• detailed analysis of cellular composition revealed an increase of differentiated cell types in the small intestine
• however, gross morphology is normal with respect to villi length, number of crypts, and number of cells per crypt
• adult mice show a ~2-fold increase in the number of MUC2-positive goblet cells in the villi of the small intestine relative to controls
• however, the number of goblet cells in the crypts of the small intestine are normal
• adult mice show an increased number of lysozyme (LYZ)-positive Paneth cells in the crypts of the small intestine (4-5 cells per crypt) relative to controls (3 cells per crypt)

nervous system
• adult mice exhibit impaired neuron differentiation in the cerebral cortex
• at 4 months of age, later born (SATB2-positive) neurons appear more scattered within the cortical plate
• adult mice display a smaller and less densely packed cerebral cortex relative to controls
• immunohistochemistry revealed less differentiated cortical cells and impaired layering on coronal sections
• however, the localization and distribution of intermediate precursor cells (IPC) in the subventricular zone is normal
• at 4 months of age, layering of the deep-layer (CTIP2-positive, layer V-VI) and upper-layer glutamatergic neurons (SATB2-positive, layer II-IV) is impaired relative to controls

cellular
• adult mice show a ~2-fold increase in the number of MUC2-positive goblet cells in the villi of the small intestine relative to controls
• however, the number of goblet cells in the crypts of the small intestine are normal
• adult mice exhibit impaired cell differentiation in the small intestine epithelium and in neurons in the cerebral cortex
• however, levels of histone H2B and monoubiquitination of histone H2B (H2Bub1) remain constant in protein samples isolated from mutant tissues
• adult mice exhibit impaired neuron differentiation in the cerebral cortex

endocrine/exocrine glands
• adult mice show an increased number of lysozyme (LYZ)-positive Paneth cells in the crypts of the small intestine (4-5 cells per crypt) relative to controls (3 cells per crypt)




Genotype
MGI:5706121
ht3
Allelic
Composition
Usp22tm1a(KOMP)Wtsi/Usp22+
Genetic
Background
C57BL/6N-Usp22tm1a(KOMP)Wtsi/Wtsi
Cell Lines EPD0119_2_D11
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Usp22tm1a(KOMP)Wtsi mutation (3 available); any Usp22 mutation (33 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body

hematopoietic system





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory