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Symbol
Name
ID
Loxhd1
lipoxygenase homology domains 1
MGI:1914609
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Eye movement-induced pain
Disease(s) Associated with LOXHD1
Fuchs' endothelial dystrophy

Mouse Phenotypes
decreased startle reflex
Availability Mouse Genotype
Loxhd1sba/Loxhd1sba

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
07/02/2024
MGI 6.13
The Jackson Laboratory