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Symbol
Name
ID
Ddr2
discoidin domain receptor family, member 2
MGI:1345277
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Calcification of falx cerebri
Spinal cord compression
Syringomyelia
Global developmental delay
Motor delay
Disease(s) Associated with DDR2
spondylometaepiphyseal dysplasia, short limb-hand type

Mouse Phenotypes
small pituitary gland
Availability Mouse Genotype
Ddr2slie/Ddr2slie

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