Symbol Name ID |
Intu
inturned planar cell polarity protein MGI:2443752 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | CNS hypomyelination |
Ventriculomegaly |
Delayed speech and language development |
Disease(s) Associated with INTU | |||
orofaciodigital syndrome XVII |
Mouse Phenotypes | nervous system phenotype |
abnormal embryonic neuroepithelium primary cilium morphology |
absent floor plate |
small floor plate |
abnormal cranial flexure morphology |
diencephalon hyperplasia |
telencephalon hypoplasia |
exencephaly |
abnormal motor neuron morphology |
abnormal ventral interneuron 3 morphology |
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Availability | Mouse Genotype | ||||||||||
Intudtm/Intudtm | * | ||||||||||
Intutm1.2Aliu/Intutm1.2Aliu |
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 07/05/2024 MGI 6.24 |
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