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Symbol Name ID |
Nkx6-2
NK6 homeobox 2 MGI:1352738 |
| Darker colors indicate more annotations |
| Human Phenotypes | Torticollis |
Spasticity |
CNS hypomyelination |
Leukodystrophy |
Cerebellar atrophy |
Limb ataxia |
Truncal ataxia |
Head titubation |
Abnormal pyramidal sign |
Dysarthria |
Cognitive impairment |
Hyperreflexia |
Limb dystonia |
Severe global developmental delay |
Motor delay |
| Disease(s) Associated with NKX6-2 | |||||||||||||||
| spastic ataxia 8 |
| Mouse Phenotypes | abnormal optic nerve morphology |
axon degeneration |
abnormal myelination |
abnormal nerve conduction |
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| Availability | Mouse Genotype | ||||
| Nkx6-2tm1Gow/Nkx6-2tm1Gow | |||||
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 |
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