|
Symbol Name ID |
Tmem216
transmembrane protein 216 MGI:1920020 |
| Darker colors indicate more annotations |
| Human Phenotypes | Iris coloboma |
Chorioretinal coloboma |
Optic disc coloboma |
Retinal dystrophy |
Hypertelorism |
Microphthalmia |
Strabismus |
Esotropia |
Nystagmus |
Rotary nystagmus |
Abnormal saccadic eye movements |
Abnormality of ocular smooth pursuit |
Impaired smooth pursuit |
Oculomotor apraxia |
Visual impairment |
Ptosis |
| Disease(s) Associated with TMEM216 | ||||||||||||||||
| Joubert syndrome | ||||||||||||||||
| Joubert syndrome 2 | ||||||||||||||||
| Meckel syndrome 2 |
| Mouse Phenotypes | abnormal lens development |
anophthalmia |
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| Availability | Mouse Genotype | ||
| Tmem216em1Cya/Tmem216em1Cya | |||
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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