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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Arfip2tm1d(EUCOMM)Wtsi
targeted mutation 1d, Wellcome Trust Sanger Institute
MGI:7611851
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Arfip2tm1d(EUCOMM)Wtsi/Arfip2tm1d(EUCOMM)Wtsi involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N * CBA MGI:7611853


Genotype
MGI:7611853
hm1
Allelic
Composition
Arfip2tm1d(EUCOMM)Wtsi/Arfip2tm1d(EUCOMM)Wtsi
Genetic
Background
involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Arfip2tm1d(EUCOMM)Wtsi mutation (0 available); any Arfip2 mutation (21 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
renal/urinary system
N
• mice do not show any developmental abnormalities or changes in kidney/body weight and exhibit no increase in proteinuria levels after 18 months
• mice with STZ-induced type I diabetic nephropathy show increased albumin/creatinine ratio
• podocyte foot processes show an increase in widening and misconfiguration in mice with STZ-induced type I diabetic nephropathy compared to controls
• mice with STZ-induced type I diabetic nephropathy show decreased slit diaphragm density and slit diaphragms that are partially translocated to proximal parts of food processes compared to controls

homeostasis/metabolism
• autophagy is impaired in mice with STZ-induced type I diabetic nephropathy
• mice with STZ-induced type I diabetic nephropathy show increased albumin/creatinine ratio
• mice intraperitoneally injected with streptozotocin (STZ) to induce type I diabetes develop increased albuminuria and mild nephropathy (glomerular hypertrophy, hyperfiltration) but no differences in kidney weight/body weight ratios, in blood glucose levels, or in glomerular sclerosis compared to controls

cellular
• autophagy is impaired in mice with STZ-induced type I diabetic nephropathy





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last database update
09/24/2024
MGI 6.24
The Jackson Laboratory