Symbol Name ID |
Tctn2
tectonic family member 2 MGI:1915228 |
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 |
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Availability | Mouse Genotype | |
Tctn2tm1.1Reit/Tctn2tm1.1Reit |
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 04/30/2024 MGI 6.23 |
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