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Symbol
Name
ID

Crls1
cardiolipin synthase 1
MGI:1913836

Phenotype annotations related to mortality/aging

Darker colors indicate more annotations

Human Phenotypes	Death in infancy	Neonatal death
Disease(s) Associated with CRLS1	Death in infancy	Neonatal death
combined oxidative phosphorylation deficiency 57

Mouse Phenotypes		lethality throughout fetal growth and development, complete penetrance	preweaning lethality, complete penetrance
Availability	Mouse Genotype
	Crls1^{tm1a(EUCOMM)Wtsi}/Crls1^{tm1a(EUCOMM)Wtsi}

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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