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Symbol
Name
ID

Mpv17
MpV17 mitochondrial inner membrane protein
MGI:97138

Phenotype annotations related to muscle

Darker colors indicate more annotations

Human Phenotypes	Foot dorsiflexor weakness	Hypotonia	EMG: chronic denervation signs	Distal muscle weakness	Progressive muscle weakness	Skeletal muscle atrophy	Distal amyotrophy
Disease(s) Associated with MPV17	Foot dorsiflexor weakness	Hypotonia	EMG: chronic denervation signs	Distal muscle weakness	Progressive muscle weakness	Skeletal muscle atrophy	Distal amyotrophy
Charcot-Marie-Tooth disease type 2EE
mitochondrial DNA depletion syndrome 6

Mouse Phenotypes		decreased muscle fiber mitochondrial DNA content	abnormal hypodermis muscle layer 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