Symbol Name ID |
Ntn1
netrin 1 MGI:105088 |
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 |
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Availability | Mouse Genotype | |||
Ntn1Gt(IRESBetageo)1Pgr/Ntn1Gt(IRESBetageo)1Pgr | ||||
Ntn1Gt(ST629)Byg/Ntn1Gt(ST629)Byg |
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 |
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