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Symbol
Name
ID

Mpv17
MpV17 mitochondrial inner membrane protein
MGI:97138

Phenotype annotations related to liver/biliary system

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Hepatic steatosis	Macrovesicular hepatic steatosis	Microvesicular hepatic steatosis	Hepatomegaly	Cirrhosis	Micronodular cirrhosis	Hepatocellular necrosis	Cholestasis	Jaundice	Prolonged neonatal jaundice	Hepatocellular carcinoma
Disease(s) Associated with MPV17	Hepatic steatosis	Macrovesicular hepatic steatosis	Microvesicular hepatic steatosis	Hepatomegaly	Cirrhosis	Micronodular cirrhosis	Hepatocellular necrosis	Cholestasis	Jaundice	Prolonged neonatal jaundice	Hepatocellular carcinoma
Charcot-Marie-Tooth disease type 2EE
mitochondrial DNA depletion syndrome 6

Mouse Phenotypes		liver/biliary system phenotype	abnormal liver sinusoid morphology	decreased hepatocyte mitochondrial DNA content	abnormal liver lobule morphology	abnormal hepatocyte morphology	abnormal portal triad morphology
Availability	Mouse Genotype
	Mpv17/Mpv17	*

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/23/2024 MGI 6.23