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Symbol Name ID |
Tctn2
tectonic family member 2 MGI:1915228 |
| Darker colors indicate more annotations |
| Human Phenotypes | Anhydramnios |
| Disease(s) Associated with TCTN2 | |
| Meckel syndrome 8 |
| Mouse Phenotypes | absent embryonic cilia |
abnormal rostral-caudal axis patterning |
abnormal limb mesenchyme morphology |
abnormal embryonic neuroepithelium morphology |
absent floor plate |
open neural tube |
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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 05/19/2026 MGI 6.24 |
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