Symbol Name ID |
Tmem107
transmembrane protein 107 MGI:1914160 |
Darker colors indicate more annotations |
Human Phenotypes | Retinopathy |
Oculomotor apraxia |
Ptosis |
Disease(s) Associated with TMEM107 | |||
Meckel syndrome 13 | |||
orofaciodigital syndrome XVI |
Mouse Phenotypes | optic nerve hypoplasia |
abnormal eye development |
microphthalmia |
anophthalmia |
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Availability | Mouse Genotype | ||||
Tmem107schlei/Tmem107schlei | |||||
Tmem107tm1Lex/Tmem107tm1Lex |
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 05/14/2024 MGI 6.23 |
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