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Phenotypes Associated with This Genotype
Genotype
MGI:6368626
Allelic
Composition		 Polg2M1Rvt/Polg2+
Genetic
Background		 involves: BALB/c * C3H/HeH
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Polg2M1Rvt mutation (0 available); any Polg2 mutation (25 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
renal/urinary system
nephrocalcinosis ( J:277879 )
• calcium phosphate crystals in renal cortex and papilla

homeostasis/metabolism
homeostasis/metabolism phenotype ( J:277879 )
N
• normal urinary excretion of calcium, phosphate, oxalate, and protein
• normal plasma sodium, potassium, albumin-adjusted calcium, chloride, urea, creatinine, glucose, phosphate, and alkaline phosphatase activity levels

vision/eye
vision/eye phenotype ( J:277879 )
N
• no ocular defects

Mouse Models of Human Disease
 DO ID OMIM ID(s) Ref(s)
nephrocalcinosis DOID:12679 J:277879

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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Send questions and comments to User Support. 		last database update
11/19/2024
MGI 6.24 		The Jackson Laboratory