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Symbol
Name
ID
Casr
calcium-sensing receptor
MGI:1351351
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Optic atrophy
Disease(s) Associated with CASR
autosomal dominant hypocalcemia

Mouse Phenotypes
cataract
Availability Mouse Genotype
CasrNuf/CasrNuf
CasrNuf/Casr+

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
04/09/2024
MGI 6.23
The Jackson Laboratory