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Phenotypes Associated with This Genotype
Genotype
MGI:4436912
Allelic
Composition
Vhltm1.1Wkr/Vhl+
Genetic
Background
involves: 129S4/SvJae * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Vhltm1.1Wkr mutation (1 available); any Vhl mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• enlarged blood vessels in kidneys and adrenal glands at 12 months of age

renal/urinary system
• renal cortical microcysts found at 12 months

liver/biliary system
N
• normal liver histology at 12 months

neoplasm
• in kidney papillary cysts as a result of transplacental ENU mutagenesis

homeostasis/metabolism

growth/size/body
• renal cortical microcysts found at 12 months

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
von Hippel-Lindau disease DOID:14175 OMIM:193300
J:157369


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
11/05/2024
MGI 6.24
The Jackson Laboratory