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Symbol
Name
ID

Tctn3
tectonic family member 3
MGI:1914840

Phenotype annotations related to embryo

Darker colors indicate more annotations

Human Phenotypes	Oligohydramnios
Disease(s) Associated with TCTN3	Oligohydramnios
orofaciodigital syndrome IV

Mouse Phenotypes		decreased embryonic neuroepithelium primary cilium number	abnormal embryo size	absent floor plate
Availability	Mouse Genotype	decreased embryonic neuroepithelium primary cilium number	abnormal embryo size	absent floor plate
	Tctn3^em1(IMPC)J/Tctn3^em1(IMPC)J
	Tctn3^tm1.2Blnw/Tctn3^tm1.2Blnw

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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