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Symbol
Name
ID
Tctn2
tectonic family member 2
MGI:1915228
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Anophthalmia
Microphthalmia
Nystagmus
Hypermetropia
Disease(s) Associated with TCTN2
Joubert syndrome 24
Meckel syndrome 8

Mouse Phenotypes
microphthalmia
Availability Mouse Genotype
Tctn2tm1.1Reit/Tctn2tm1.1Reit

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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last database update
01/12/2022
MGI 6.17
The Jackson Laboratory