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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Agrntm1Rwb
targeted mutation 1, Robert W Burgess
MGI:3579476
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Agrntm1Rwb/Agrntm1Rwb
Tg(APPswe,PSEN1dE9)85Dbo/?
Tg(Tek-cre)1Ywa/?
involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6 * SJL MGI:5692156
cn2
Agrntm1Rwb/Agrntm1Rwb
Tg(NPHS2-cre)295Lbh/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3716770
cn3
Agrntm1Rwb/Agrntm1Rwb
Tg(Pax3-cre)1Joe/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL MGI:3716768
cn4
Agrntm1Rwb/Agrntm1Rwb
Tg(Tek-cre)1Ywa/?
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL MGI:5692155


Genotype
MGI:5692156
cn1
Allelic
Composition
Agrntm1Rwb/Agrntm1Rwb
Tg(APPswe,PSEN1dE9)85Dbo/?
Tg(Tek-cre)1Ywa/?
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Agrntm1Rwb mutation (1 available); any Agrn mutation (101 available)
Tg(APPswe,PSEN1dE9)85Dbo mutation (6 available)
Tg(Tek-cre)1Ywa mutation (6 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• elevated Amyloid beta in females mice

homeostasis/metabolism
• elevated Amyloid beta in females mice




Genotype
MGI:3716770
cn2
Allelic
Composition
Agrntm1Rwb/Agrntm1Rwb
Tg(NPHS2-cre)295Lbh/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Agrntm1Rwb mutation (1 available); any Agrn mutation (101 available)
Tg(NPHS2-cre)295Lbh mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
renal/urinary system
N
• when compared to normal controls, no pathological changes are detected until at least 8 months of age
• glomerular filtration barrier is not compromised in mutants, with normal urinary protein and creatinine levels up to 10 months of age when compared to controls
• at ~4 months of age, glomerular basement membrane (GBM) abnormalities including focal thickening and epithelial protrusions of GBM material are observed in mutants
• focal thickening of the GBM is noted at ~4 months of age




Genotype
MGI:3716768
cn3
Allelic
Composition
Agrntm1Rwb/Agrntm1Rwb
Tg(Pax3-cre)1Joe/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Agrntm1Rwb mutation (1 available); any Agrn mutation (101 available)
Tg(Pax3-cre)1Joe mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

nervous system
• diaphragms lack neuromuscular junctions

muscle
• diaphragms lack neuromuscular junctions




Genotype
MGI:5692155
cn4
Allelic
Composition
Agrntm1Rwb/Agrntm1Rwb
Tg(Tek-cre)1Ywa/?
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Agrntm1Rwb mutation (1 available); any Agrn mutation (101 available)
Tg(Tek-cre)1Ywa mutation (6 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• expression of the Agrn gene is restricted to endothelial cells
• no obvious failure of integrity in the blood-brain barrier

cardiovascular system
• decreased diameter of microvessels





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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory