Symbol Name ID |
Tmem218
transmembrane protein 218 MGI:1913529 |
Darker colors indicate more annotations |
Human Phenotypes | Iris coloboma |
Strabismus |
Nystagmus |
Oculomotor apraxia |
Ptosis |
Disease(s) Associated with TMEM218 | |||||
Joubert syndrome |
Mouse Phenotypes | thin retina outer nuclear layer |
increased susceptibility to age-related retinal degeneration |
abnormal electroretinogram waveform feature |
abnormal vision |
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Availability | Mouse Genotype | ||||
Tmem218Gt(OST40451)Lex/Tmem218Gt(OST40451)Lex |
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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