Symbol Name ID |
Tmem107
transmembrane protein 107 MGI:1914160 |
Darker colors indicate more annotations |
Human Phenotypes | Occipital encephalocele |
Oculomotor apraxia |
Ventriculomegaly |
Cerebellar hypoplasia |
Molar tooth sign on MRI |
Gray matter heterotopia |
Ataxia |
Intellectual disability |
Intellectual disability, severe |
Inability to walk |
Global developmental delay |
Motor delay |
Disease(s) Associated with TMEM107 | ||||||||||||
Meckel syndrome 13 | ||||||||||||
orofaciodigital syndrome XVI |
Mouse Phenotypes | abnormal vomeronasal organ morphology |
abnormal neural tube morphology |
absent floor plate |
exencephaly |
optic nerve hypoplasia |
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Availability | Mouse Genotype | |||||
Tmem107schlei/Tmem107schlei | ||||||
Tmem107tm1Lex/Tmem107tm1Lex | ||||||
Tmem107schlei/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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