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Symbol
Name
ID
Dcc
DCC netrin 1 receptor
MGI:94869
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Myalgia
Disease(s) Associated with DCC
congenital mirror movement disorder

Mouse Phenotypes
abnormal suckling behavior
ataxia
abnormal gait
Availability Mouse Genotype
Dcckanga/Dcckanga
Dcctm1Wbg/Dcctm1Wbg
Dcckanga/Dcctm1Wbg

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