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Symbol Name ID |
Tctn2
tectonic family member 2 MGI:1915228 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Encephalocele |
Occipital encephalocele |
Increased circulating prolactin concentration |
Pituitary hypothyroidism |
Spasticity |
Pachygyria |
Polymicrogyria |
Cerebellar hypoplasia |
Ataxia |
Dysmetria |
Clumsiness |
Depression |
Lethargy |
Attention deficit hyperactivity disorder |
Absent speech |
Hyporeflexia |
Hyperreflexia |
Gait disturbance |
Neurodevelopmental delay |
Global developmental delay |
| Disease(s) Associated with TCTN2 | |||||||||||||||||||||
| Joubert syndrome 24 | |||||||||||||||||||||
| Meckel syndrome 8 |
| Mouse Phenotypes | abnormal embryonic neuroepithelium morphology |
absent floor plate |
open neural tube |
exencephaly |
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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 07/08/2026 MGI 6.24 |
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