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Symbol
Name
ID
Ntn1
netrin 1
MGI:105088
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Myalgia
Disease(s) Associated with NTN1
congenital mirror movement disorder

Mouse Phenotypes
absent gastric milk in neonates
abnormal righting response
abnormal locomotor coordination
Availability Mouse Genotype
Ntn1Gt(IRESBetageo)1Pgr/Ntn1Gt(IRESBetageo)1Pgr
Ntn1Gt(ST629)Byg/Ntn1Gt(ST629)Byg

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
04/30/2024
MGI 6.23
The Jackson Laboratory