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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Mep1btm1Bond
targeted mutation 1, Judith S Bond
MGI:2450870
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Mep1btm1Bond/Mep1btm1Bond B6.129-Mep1btm1Bond MGI:3833919
hm2
Mep1btm1Bond/Mep1btm1Bond involves: 129S1/Sv * 129X1/SvJ MGI:2450872
hm3
Mep1btm1Bond/Mep1btm1Bond involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:5439494


Genotype
MGI:3833919
hm1
Allelic
Composition
Mep1btm1Bond/Mep1btm1Bond
Genetic
Background
B6.129-Mep1btm1Bond
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mep1btm1Bond mutation (0 available); any Mep1b mutation (44 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
N
• similar blood urea nitrogen response to non-lethal ip injection with E. coli lipopolysaccharide to that seen in controls
• similar circulating creatinine response to non-lethal ip injection with E. coli lipopolysaccharide to that seen in controls
• similar hypothermia response to non-lethal ip injection with E. coli lipopolysaccharide to that seen in controls
• lipopolysaccharide induced initial elevation in nitrite/nitrate levels is similar to that of controls but more intense

immune system
N
• proinflammatory cytokine response to non-lethal ip injection with E. coli lipopolysaccharide similar to that of controls




Genotype
MGI:2450872
hm2
Allelic
Composition
Mep1btm1Bond/Mep1btm1Bond
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mep1btm1Bond mutation (0 available); any Mep1b mutation (44 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• partial embryonic lethality; reduced proportion (12%) of homozygous null F2 animals observed at birth

growth/size/body
• increased body weight at time of birth; females display increased body weight at time of weaning, but body weight was not statistically different at 150 days of age

reproductive system




Genotype
MGI:5439494
hm3
Allelic
Composition
Mep1btm1Bond/Mep1btm1Bond
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mep1btm1Bond mutation (0 available); any Mep1b mutation (44 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• at 6 to 24 hrs after kidney I/R injury, male homozygotes exhibit significantly lower plasma creatinine levels than similarly treated wild-type controls
• at 6 to 72 hrs after kidney I/R injury, male homozygotes exhibit significantly lower BUN levels than similarly treated wild-type controls
• at 6 and 24 hrs after kidney I/R injury, male homozygotes exhibit significantly lower urinary cytokine (CXCL1 and IL-6) levels relative to similarly treated wild-type controls
• following kidney ischemia-reperfusion (I/R) injury, male homozygotes exhibit no death at 24-48 hrs post-injury, better preservation of renal function (as shown by lower BUN values at all time points), a less severe inflammatory response, and less disruption and shedding of membranes in proximal tubules cells relative to similarly treated wild-type controls

immune system
• following kidney I/R injury, male homozygotes exhibit decreased leukocyte infiltration and reduced expression of inflammatory markers in the kidney relative to similarly treated wild-type controls

renal/urinary system
• at 6 and 24 hrs after kidney I/R injury, male homozygotes exhibit significantly lower urinary cytokine (CXCL1 and IL-6) levels relative to similarly treated wild-type controls
• following kidney ischemia-reperfusion (I/R) injury, male homozygotes exhibit no death at 24-48 hrs post-injury, better preservation of renal function (as shown by lower BUN values at all time points), a less severe inflammatory response, and less disruption and shedding of membranes in proximal tubules cells relative to similarly treated wild-type controls
• at 96 hrs after kidney I/R injury, male homozygotes display significantly less brush-border disruption and collapse than wild-type controls, with less than 10% of tubules containing detached DPPIV staining material





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