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Phenotypes Associated with This Genotype
Genotype
MGI:4437767
Allelic
Composition
Tg(Pkd1)6Mtru/0
Genetic
Background
involves: C57BL/6J * CBA/J
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
mortality/aging
• mice die around 17 months of age

renal/urinary system
• proliferation of kidney cells is increased compared to in wild-type mice
• at 1 month of age, mice exhibit scattered tubular microcysts unlike wild-type mice
• at 9 months, mice develop cysts unlike wild-type mice
• by 12 to 16 months, mice exhibit severe cysts unlike wild-type mice
• mice develop cysts in the medulla, cortex and glomeruli unlike wild-type mice
• mice develop hemorrhagic cysts unlike wild-type mice
• cysts exhibit proteinaceous casts in tubular cysts and interstitial fibrosis unlike wild-type mice
• cysts originate from the proximal and collecting ducts and glomeruli unlike in wild-type mice
• cysts exhibit calcium deposits
• bilateral
• at 15 months, urine creatinine content is reduced compared to in wild-type mice
• at 4 months, mice exhibit non-selective proteinuria unlike wild-type mice
• at 15 months, urine nitrogen content is reduced compared to in wild-type mice
• partial and total
• cystic and non-cystic tubules exhibit epithelial hyperplasia and hypertrophy with occasional polyps of varying severity unlike wild-type mice
• at 1 month of age
• at 7 to 16 months
• at 1 month, mice exhibit mild tubular dilation unlike wild-type mice
• at 7 months mice develop glomerular and tubular dilation unlike wild-type mice
• proteinaceous casts in tubular cysts
• calcium deposits were limited to the renal papilla
• at 15 months

cardiovascular system
• thickness is increased
• mice exhibit evidence of eccentric dilated cardiac hypertrophy
• left ventricular wall systolic and diastolic thickness are increased compared to in wild-type mice indicating hypertrophy
• aortic valve leaflets are opaque rather than translucent as in wild-type mice
• left ventricular wall systolic and diastolic thickness are increased compared to in wild-type mice indicating hypertrophy
• aortic root diameter and area are increased compared to in wild-type mice
• mice exhibit increased fractional ejection and shortening compared with wild-type mice

liver/biliary system
• in 1 in 32 mice, likely of cholangiocye origins, and affecting preferentially female mice
• mice exhibit broad band fibrosis along intrahepatic ducts unlike wild-type mice
• hepatic fibrosis is 4- to 5-fold greater than in wild-type mice

hematopoietic system
• at 15 months

homeostasis/metabolism
• at 15 months, urine creatinine content is reduced compared to in wild-type mice
• at 4 months, mice exhibit non-selective proteinuria unlike wild-type mice
• at 15 months, urine nitrogen content is reduced compared to in wild-type mice

muscle
• left ventricular wall systolic and diastolic thickness are increased compared to in wild-type mice indicating hypertrophy
• mice exhibit increased fractional ejection and shortening compared with wild-type mice

cellular
• proliferation of kidney cells is increased compared to in wild-type mice

growth/size/body
• mice exhibit evidence of eccentric dilated cardiac hypertrophy
• left ventricular wall systolic and diastolic thickness are increased compared to in wild-type mice indicating hypertrophy
• at 1 month of age, mice exhibit scattered tubular microcysts unlike wild-type mice
• at 9 months, mice develop cysts unlike wild-type mice
• by 12 to 16 months, mice exhibit severe cysts unlike wild-type mice
• mice develop cysts in the medulla, cortex and glomeruli unlike wild-type mice
• mice develop hemorrhagic cysts unlike wild-type mice
• cysts exhibit proteinaceous casts in tubular cysts and interstitial fibrosis unlike wild-type mice
• cysts originate from the proximal and collecting ducts and glomeruli unlike in wild-type mice
• cysts exhibit calcium deposits
• bilateral
• in 1 in 32 mice, likely of cholangiocye origins, and affecting preferentially female mice


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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory