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Symbol Name ID |
Ntn1
netrin 1 MGI:105088 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Bimanual synkinesia |
| Disease(s) Associated with NTN1 | |
| mirror movements 4 |
| Mouse Phenotypes | nervous system phenotype |
abnormal axon guidance |
abnormal sensory neuron axon guidance |
abnormal brain commissure morphology |
absent corpus callosum |
absent hippocampal commissure |
abnormal anterior commissure morphology |
abnormal pyramidal decussation morphology |
abnormal pontine nuclei morphology |
abnormal spinal cord ependymal layer morphology |
abnormal corticospinal tract morphology |
abnormal spinal cord ventral commissure morphology |
abnormal dorsal spinal root morphology |
abnormal spinal cord central canal morphology |
abnormal spinal cord dorsal column morphology |
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| Availability | Mouse Genotype | |||||||||||||||
| Ntn1Gt(IRESBetageo)1Pgr/Ntn1Gt(IRESBetageo)1Pgr | ||||||||||||||||
| Ntn1Gt(ST629)Byg/Ntn1Gt(ST629)Byg | * | |||||||||||||||
| Ntn1tm1.2Tek/Ntn1tm1.2Tek | ||||||||||||||||
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 01/20/2026 MGI 6.24 |
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