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Symbol
Name
ID

Lonp1
lon peptidase 1, mitochondrial
MGI:1921392

Phenotype annotations related to growth/size/body

Darker colors indicate more annotations

Human Phenotypes	Omphalocele	Umbilical hernia	Short stature
Disease(s) Associated with LONP1
CODAS syndrome

Mouse Phenotypes		embryonic growth retardation	decreased embryo size	increased lean body mass
Availability	Mouse Genotype	embryonic growth retardation	decreased embryo size	increased lean body mass
	Lonp1^tm1Otin/Lonp1^tm1Otin
	Lonp1^{tm1b(EUCOMM)Hmgu}/Lonp1⁺

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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