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Symbol
Name
ID
Tmem107
transmembrane protein 107
MGI:1914160
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Occipital encephalocele
Oculomotor apraxia
Cerebellar hypoplasia
Molar tooth sign on MRI
Ventriculomegaly
Gray matter heterotopia
Ataxia
Inability to walk
Intellectual disability
Intellectual disability, severe
Global developmental delay
Disease(s) Associated with TMEM107
Meckel syndrome 13
orofaciodigital syndrome XVI

Mouse Phenotypes
abnormal neural tube morphology
absent floor plate
exencephaly
Availability Mouse Genotype
Tmem107schlei/Tmem107schlei
Tmem107tm1Lex/Tmem107tm1Lex
Tmem107schlei/Tmem107tm1Lex

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO)
Citing These Resources
Funding Information
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last database update
05/14/2019
MGI 6.14
The Jackson Laboratory