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Symbol
Name
ID

Tctn3
tectonic family member 3
MGI:1914840

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Hypertelorism	Proptosis	Abnormality of eye movement
Disease(s) Associated with TCTN3	Hypertelorism	Proptosis	Abnormality of eye movement
Joubert syndrome 18
orofaciodigital syndrome IV

Mouse Phenotypes		anophthalmia
Availability	Mouse Genotype	anophthalmia
	Tctn3^em1(IMPC)J/Tctn3^em1(IMPC)J

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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