Symbol Name ID |
Mnx1
motor neuron and pancreas homeobox 1 MGI:109160 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Tethered cord |
Global developmental delay |
Disease(s) Associated with MNX1 | ||
Currarino syndrome |
Mouse Phenotypes | nervous system phenotype |
abnormal axon guidance |
abnormal innervation |
abnormal motor neuron morphology |
abnormal axon morphology |
abnormal neuromuscular synapse morphology |
abnormal hypoglossal nerve morphology |
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Availability | Mouse Genotype | |||||||
Mnx1tm1Jhk/Mnx1tm1Jhk | ||||||||
Mnx1tm1Tmj/Mnx1tm1Tmj | * | |||||||
Mnx1tm2Tmj/Mnx1tm2Tmj | * | |||||||
Mnx1tm3Tmj/Mnx1tm3Tmj | * | |||||||
Mnx1tm4(cre)Tmj/Mnx1+ |
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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