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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Apptm2Cwe
targeted mutation 2, Charles Weissmann
MGI:2154535
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Apptm2Cwe/Apptm2Cwe involves: 129P2/OlaHsd * 129S/SvEv MGI:2176996
hm2
Apptm2Cwe/Apptm2Cwe involves: 129P2/OlaHsd * C57BL/6 MGI:3590206
ht3
Apptm3.2Umu/Apptm2Cwe involves: 129P2/OlaHsd * BALB/cJ * C57BL/6N MGI:4822179
cx4
Aplp2tm1Dbo/Aplp2tm1Dbo
Apptm2Cwe/Apptm2Cwe
involves: 129/Sv * 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * C57BL/6J MGI:2176994
cx5
Aplp1tm1Umu/Aplp1tm1Umu
Apptm2Cwe/Apptm2Cwe
involves: 129/Sv * 129P2/OlaHsd * C57BL/6 MGI:2176990


Genotype
MGI:2176996
hm1
Allelic
Composition
Apptm2Cwe/Apptm2Cwe
Genetic
Background
involves: 129P2/OlaHsd * 129S/SvEv
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apptm2Cwe mutation (0 available); any App mutation (103 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• brain weight is reduced 10% relative to controls
• Background Sensitivity: greatly increased frequency of absent corpus callosum over controls in 129-derived genetic backgrounds
• Background Sensitivity: greatly reduced ventral hippocampal commissure; 83% reduced compared to controls
• reduced size of anterior commissure, independent of genetic background




Genotype
MGI:3590206
hm2
Allelic
Composition
Apptm2Cwe/Apptm2Cwe
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apptm2Cwe mutation (0 available); any App mutation (103 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• brain weight is reduced 10% relative to controls
• Background Sensitivity: 4-11% smaller than controls; absence of corpus callosum is not statistically significant in mutant lines with greater than 50% C57BL/6 genetic background contribution when compared to controls
• Background Sensitivity: reduced ventral hippocampal commissure; comparable to the size reduction in Apptm1Cwe mutant mice on a mixed C57BL/6 and 129S2/SvPas genetic background




Genotype
MGI:4822179
ht3
Allelic
Composition
Apptm3.2Umu/Apptm2Cwe
Genetic
Background
involves: 129P2/OlaHsd * BALB/cJ * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apptm2Cwe mutation (0 available); any App mutation (103 available)
Apptm3.2Umu mutation (0 available); any App mutation (103 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• displayed a pronounced and significant difference in grip strength compared to wild-type mice

growth/size/body
• body weight is reduced by about 10.6%

nervous system
• wet brain weight is reduced




Genotype
MGI:2176994
cx4
Allelic
Composition
Aplp2tm1Dbo/Aplp2tm1Dbo
Apptm2Cwe/Apptm2Cwe
Genetic
Background
involves: 129/Sv * 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Aplp2tm1Dbo mutation (1 available); any Aplp2 mutation (32 available)
Apptm2Cwe mutation (0 available); any App mutation (103 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• no defect detected grossly or microscopically
• no animals survive to weaning age




Genotype
MGI:2176990
cx5
Allelic
Composition
Aplp1tm1Umu/Aplp1tm1Umu
Apptm2Cwe/Apptm2Cwe
Genetic
Background
involves: 129/Sv * 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Aplp1tm1Umu mutation (0 available); any Aplp1 mutation (26 available)
Apptm2Cwe mutation (0 available); any App mutation (103 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• 10% decrease in body weight at 9 weeks of age





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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory