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Symbol
Name
ID

Intu
inturned planar cell polarity protein
MGI:2443752

Phenotype annotations related to nervous system

*	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
Availability	Mouse Genotype	nervous system phenotype		absent floor plate	small floor plate	abnormal cranial flexure morphology	diencephalon hyperplasia	telencephalon hypoplasia	exencephaly	abnormal motor neuron morphology	abnormal ventral interneuron 3 morphology
	Intu^dtm/Intu^dtm	*
	Intu^tm1.2Aliu/Intu^tm1.2Aliu

Contributing Projects: 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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