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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Becn1tm2.1Blev
targeted mutation 2.1, Beth Levine
MGI:6156896
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Becn1tm2.1Blev/Becn1tm2.1Blev B6.129-Becn1tm2.1Blev MGI:6257017
cx2
Becn1tm2.1Blev/Becn1tm2.1Blev
Tg(APPV717F)109Ili/0
B6.Cg-Becn1tm2.1Blev Tg(APPV717F)109Ili MGI:6257023
cx3
Becn1tm2.1Blev/Becn1tm2.1Blev
Tg(CAG-EGFP/Map1lc3b)53Nmz/0
involves: 129 * C57BL/6 * C57BL/6J * C57BL/6NCrlj * DBA/2 MGI:6257019
cx4
Becn1tm2.1Blev/Becn1tm2.1Blev
Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/0
involves: 129 * C57BL/6 * C57BL/6J * SJL MGI:6257020


Genotype
MGI:6257017
hm1
Allelic
Composition
Becn1tm2.1Blev/Becn1tm2.1Blev
Genetic
Background
B6.129-Becn1tm2.1Blev
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Becn1tm2.1Blev mutation (1 available); any Becn1 mutation (36 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• mice are fertile, of normal size and weight, and show normal histology in major organs




Genotype
MGI:6257023
cx2
Allelic
Composition
Becn1tm2.1Blev/Becn1tm2.1Blev
Tg(APPV717F)109Ili/0
Genetic
Background
B6.Cg-Becn1tm2.1Blev Tg(APPV717F)109Ili
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Becn1tm2.1Blev mutation (1 available); any Becn1 mutation (36 available)
Tg(APPV717F)109Ili mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice exhibit decreased mortality compared to single Tg(APPV717F)109Ili expressing mice




Genotype
MGI:6257019
cx3
Allelic
Composition
Becn1tm2.1Blev/Becn1tm2.1Blev
Tg(CAG-EGFP/Map1lc3b)53Nmz/0
Genetic
Background
involves: 129 * C57BL/6 * C57BL/6J * C57BL/6NCrlj * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Becn1tm2.1Blev mutation (1 available); any Becn1 mutation (36 available)
Tg(CAG-EGFP/Map1lc3b)53Nmz mutation (5 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• under fed and resting conditions, mice exhibit a higher number of autophagosomes in skeletal muscle and brain, indicating high basal autophagy

homeostasis/metabolism
• under fed and resting conditions, mice exhibit a higher number of autophagosomes in skeletal muscle and brain, indicating high basal autophagy




Genotype
MGI:6257020
cx4
Allelic
Composition
Becn1tm2.1Blev/Becn1tm2.1Blev
Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/0
Genetic
Background
involves: 129 * C57BL/6 * C57BL/6J * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Becn1tm2.1Blev mutation (1 available); any Becn1 mutation (36 available)
Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• mice show improved performance day by day in both the escape latency and distance during the hidden platform trails of the Morris water maze compared to single Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas expressing mice

homeostasis/metabolism
• mice show lower levels of both soluble and insoluble amyloid beta 42 in the brain than in single Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas expressing mice
• however, expression of the precursor APP remains unaffected
• mice show a reduction of amyloid plaques in the cortex and a trend of reduction in the hippocampus
• short-term treatment of mice with SBI-0206965, an autophagy inhibitor blocking the kinase activity of an essential upstream kinase ULK1, abolishes the reduction in brain amyloid beta 42 levels

nervous system
• mice show lower levels of both soluble and insoluble amyloid beta 42 in the brain than in single Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas expressing mice
• however, expression of the precursor APP remains unaffected
• mice show a reduction of amyloid plaques in the cortex and a trend of reduction in the hippocampus
• short-term treatment of mice with SBI-0206965, an autophagy inhibitor blocking the kinase activity of an essential upstream kinase ULK1, abolishes the reduction in brain amyloid beta 42 levels





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