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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Kdr-AGER)102Hyam
transgene insertion 102, Hiroshi Yamamoto
MGI:3696984
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Tg(Ins2-Nos2)40Okam/0
Tg(Kdr-AGER)102Hyam/0
involves: C57BL/6J * CBA/J * CD-1 * DBA/2 MGI:3706554


Genotype
MGI:3706554
cx1
Allelic
Composition
Tg(Ins2-Nos2)40Okam/0
Tg(Kdr-AGER)102Hyam/0
Genetic
Background
involves: C57BL/6J * CBA/J * CD-1 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• serum creatinine levels increase to 1.24 mg/dl
• treatment with an inhibitor of AGE formation improves serum creatinine levels at 6 months
• mice show hyperglycemia (and elevated serum HbA1c) by 2 months of age, indicative of a diabetic condition
• serum albumin/creatinine ratio becomes significantly higher at 4 months

renal/urinary system
• glomerular cell proliferation is accelerated in double transgenics compared to controls
• kidney weight to body weight ratios in double transgenic mice are increased compared to Tg(Ins2-Nos2)40Okam single transgenic mice
• serum albumin/creatinine ratio becomes significantly higher at 4 months
• treatment with an inhibitor of advanced glycation end product (AGE) formation suppresses diabetic nephropathy; AGE levels in blood in double transgenic and single transgenic diabetic controls are reduced ~to levels in nondiabetic animals
• Tg(Ins2-Nos2)40Okam single transgenic controls and double transgenic kidneys display mesangial expansion compared to controls; at 4 months, severity is greater in double transgenic mice with ~50 glomeruli/mouse showing increases in mesangium area, mesangium fraction, and sclerosis index
• lesions observed double transgenic or Tg(Ins2-Nos2)40Okam single transgenic controls include glomerular cell proliferation and glomerular hypertrophy; these pathological features are accelerated in double transgenics compared to controls

cardiovascular system
• nodular lesions are observed in kidneys at 8 months of age
• treatment with an inhibitor of AGE formation improves sclerosis index at 6 months
• nodular lesions are observed in kidneys at 8 months of age

cellular
• glomerular cell proliferation is accelerated in double transgenics compared to controls

growth/size/body
• kidney weight to body weight ratios in double transgenic mice are increased compared to Tg(Ins2-Nos2)40Okam single transgenic mice

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
type 1 diabetes mellitus DOID:9744 OMIM:222100
J:70495





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