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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Lin7ctm1Dsb
targeted mutation 1, David S Bredt
MGI:3611209
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Lin7ctm1Dsb/Lin7ctm1Dsb involves: 129S1/Sv * 129X1/SvJ MGI:3804962
cx2
Lin7atm1Dsb/Lin7atm1Dsb
Lin7btm1Dsb/Lin7btm1Dsb
Lin7ctm1Dsb/Lin7ctm1Dsb
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3639323
cx3
Lin7atm1Dsb/Lin7a+
Lin7btm1Dsb/Lin7btm1Dsb
Lin7ctm1Dsb/Lin7ctm1Dsb
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3639324


Genotype
MGI:3804962
hm1
Allelic
Composition
Lin7ctm1Dsb/Lin7ctm1Dsb
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lin7ctm1Dsb mutation (0 available); any Lin7c mutation (17 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Lin7ctm1Dsb/Lin7ctm1Dsb mice display renal defects

growth/size/body
• body weight of mice is decreased by 10%
• kidneys are studded with numerous cysts in the cortex and medulla
• vast majority of cysts lack tubule segment specific markers

renal/urinary system
• sodium excretion is higher than in controls with the fractional excretion percentage being 1.2% compared to 0.74% in controls
• mice only have a 3-fold gain in urine osmalirity after 12 hour water deprivation and vasopressin injection compared to a 7.2-fold response in control mice
• kidneys are studded with numerous cysts in the cortex and medulla
• vast majority of cysts lack tubule segment specific markers
• tubular epithelia lose polarity with sodium pump channels that are normally localized basolaterally being found diffusely through out the cell
• is observed in adult kidneys with extracellular matrix proteins and fibroblasts evident
• adult kidney weight is reduced by 45% compared to controls while other organs such as heart are only 10% smaller
• decreased kidney weight is observed when homozygotes are backcrossed to 129/Sv mice or C57BL/6 mice
• adult kidneys display tubular dilation and dedifferentiation of the renal tubules
• about 15% of neonates display unilateral renal agenesis
• E14.5 kidneys have a 10-fold more apoptosis underlying the renal capsule compared to controls
• this increased apoptosis is evident as early as E12.5
• creatine clearance is modestly decreased compared to controls
• urine output is more than doubled compared to controls

homeostasis/metabolism
• blood urea nitrogen levels are significantly increased compared to controls
• sodium excretion is higher than in controls with the fractional excretion percentage being 1.2% compared to 0.74% in controls
• mice only have a 3-fold gain in urine osmalirity after 12 hour water deprivation and vasopressin injection compared to a 7.2-fold response in control mice

cellular
• E14.5 kidneys have a 10-fold more apoptosis underlying the renal capsule compared to controls
• this increased apoptosis is evident as early as E12.5




Genotype
MGI:3639323
cx2
Allelic
Composition
Lin7atm1Dsb/Lin7atm1Dsb
Lin7btm1Dsb/Lin7btm1Dsb
Lin7ctm1Dsb/Lin7ctm1Dsb
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lin7atm1Dsb mutation (0 available); any Lin7a mutation (23 available)
Lin7btm1Dsb mutation (0 available); any Lin7b mutation (13 available)
Lin7ctm1Dsb mutation (0 available); any Lin7c mutation (17 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die within one hour of birth

nervous system
• in culture, neurons from triple knock out mice show reduced EPSCs relative to wild-type

respiratory system
• mice exhibit irregular, labored breathing




Genotype
MGI:3639324
cx3
Allelic
Composition
Lin7atm1Dsb/Lin7a+
Lin7btm1Dsb/Lin7btm1Dsb
Lin7ctm1Dsb/Lin7ctm1Dsb
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lin7atm1Dsb mutation (0 available); any Lin7a mutation (23 available)
Lin7btm1Dsb mutation (0 available); any Lin7b mutation (13 available)
Lin7ctm1Dsb mutation (0 available); any Lin7c mutation (17 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die during second week postnatal





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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory