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Symbol
Name
ID

Tctn1
tectonic family member 1
MGI:3603820

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Pachygyria	Cerebellar vermis hypoplasia	Molar tooth sign on MRI
Disease(s) Associated with TCTN1
Joubert syndrome 13

Mouse Phenotypes		abnormal embryonic neuroepithelium morphology	absent floor plate	spina bifida	small embryonic telencephalon	holoprosencephaly
Availability	Mouse Genotype	abnormal embryonic neuroepithelium morphology	absent floor plate	spina bifida	small embryonic telencephalon	holoprosencephaly
	Tctn1^em1(IMPC)Mbp/Tctn1^em1(IMPC)Mbp
	Tctn1^{Gt(KST296)Byg}/Tctn1^{Gt(KST296)Byg}
	Tctn1^em1(IMPC)Mbp/Tctn1⁺

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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