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Symbol Name ID |
Tctn3
tectonic family member 3 MGI:1914840 |
| Darker colors indicate more annotations |
| Human Phenotypes | Short stature |
Severe short stature |
Failure to thrive |
Growth delay |
Intrauterine growth retardation |
| Disease(s) Associated with TCTN3 | |||||
| Joubert syndrome 18 | |||||
| orofaciodigital syndrome IV |
| Mouse Phenotypes | abnormal embryo size |
abnormal body wall morphology |
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| Availability | Mouse Genotype | ||
| Tctn3em1(IMPC)J/Tctn3em1(IMPC)J | |||
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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