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Symbol Name ID |
Tctn2
tectonic family member 2 MGI:1915228 |
| Darker colors indicate more annotations |
| Human Phenotypes | Short neck |
Abdominal distention |
Umbilical hernia |
Failure to thrive |
Growth delay |
| Disease(s) Associated with TCTN2 | |||||
| Meckel syndrome 8 |
| Mouse Phenotypes | cleft palate |
right-sided stomach |
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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 04/23/2024 MGI 6.23 |
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