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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Pkhd1cyli
cystic liver
MGI:7568836
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Pkhd1cyli/Pkhd1cyli D2.Cg-(D4Mit42-D4Smh6b) Pkhd1cyli/EiJ MGI:7568840


Genotype
MGI:7568840
hm1
Allelic
Composition
Pkhd1cyli/Pkhd1cyli
Genetic
Background
D2.Cg-(D4Mit42-D4Smh6b) Pkhd1cyli/EiJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pkhd1cyli mutation (1 available); any Pkhd1 mutation (222 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• progressive cystic liver disease consistent with that seen in Caroli disease. This is more severe in the females than in the males.

renal/urinary system
N
• distinct from human mutations in this gene or null mouse alleles no histopathologic evidence of renal cystic disease is found in homozygotes examined between 8 and 11 weeks of age

endocrine/exocrine glands
• ductal plate malformation, irregularly shaped and variably dilated bile ducts lined with hyperplastic epithelium

liver/biliary system
• progressive cystic liver disease consistent with that seen in Caroli disease. This is more severe in the females than in the males.
• ductal plate malformation, irregularly shaped and variably dilated bile ducts lined with hyperplastic epithelium

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Caroli syndrome DOID:0081394 J:343537





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
05/14/2024
MGI 6.23
The Jackson Laboratory