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Symbol Name ID |
Tctn2
tectonic family member 2 MGI:1915228 |
| Darker colors indicate more annotations |
| Human Phenotypes | Large posterior fontanelle |
Delayed cranial suture closure |
Large sella turcica |
Microcephaly |
Encephalocele |
Occipital encephalocele |
Broad forehead |
Facial edema |
Cleft upper lip |
Cleft palate |
Macroglossia |
Depressed nasal ridge |
Depressed nasal bridge |
Short nose |
| Disease(s) Associated with TCTN2 | ||||||||||||||
| Meckel syndrome 8 |
| Mouse Phenotypes | cleft palate |
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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 03/25/2025 MGI 6.24 |
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