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Symbol
Name
ID
Ntn1
netrin 1
MGI:105088
Phenotype annotations related to endocrine/exocrine glands
Darker colors indicate more annotations
Human Phenotypes
Hypogonadotropic hypogonadism
Disease(s) Associated with NTN1
congenital mirror movement disorder

Mouse Phenotypes
abnormal mammary gland development
Availability Mouse Genotype
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
04/23/2024
MGI 6.23
The Jackson Laboratory