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Symbol
Name
ID
Crls1
cardiolipin synthase 1
MGI:1913836
Phenotype annotations related to embryo
Darker colors indicate more annotations
Human Phenotypes
Nonimmune hydrops fetalis
Fetal pleural effusion
Disease(s) Associated with CRLS1
combined oxidative phosphorylation deficiency 57

Mouse Phenotypes
abnormal chorion morphology
abnormal trophoblast layer morphology
Availability Mouse Genotype
Crls1tm1a(EUCOMM)Wtsi/Crls1tm1a(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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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory