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Phenotypes Associated with This Genotype
Genotype
MGI:3582952
Allelic
Composition
Bicc1jcpk/Bicc1jcpk
Genetic
Background
involves: 101 * C3H * T STOCK
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bicc1jcpk mutation (0 available); any Bicc1 mutation (65 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• generally die between 7 to 10 days after birth with none surviving longer than 20 days (J:27506)

renal/urinary system
• cysts are evident at birth and increase in number and size with age (J:23047)
• cysts are initially found in the inner cortical and medullary regions, by 4 days of age cysts have expanded to involve most areas of the kidney including the outer cortex, and by 7 days virtually the entire kidney is affected (J:23047)

liver/biliary system
• about 50% of homozygotes have an enlarged gallbladder

digestive/alimentary system
• dilation of the pancreatic duct

growth/size/body
• about 50% of homozygotes have an enlarged gallbladder
• cysts are evident at birth and increase in number and size with age (J:23047)
• cysts are initially found in the inner cortical and medullary regions, by 4 days of age cysts have expanded to involve most areas of the kidney including the outer cortex, and by 7 days virtually the entire kidney is affected (J:23047)
• seen at 3 to 10 days of age

endocrine/exocrine glands
• dilation of the pancreatic duct
• about 50% of homozygotes have an enlarged gallbladder

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
autosomal recessive polycystic kidney disease DOID:0110861 OMIM:263200
J:23047


Contributing Projects:
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