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Symbol
Name
ID
Tmem107
transmembrane protein 107
MGI:1914160
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Hamartoma of tongue
Short palpebral fissure
Retrognathia
Occipital encephalocele
Disease(s) Associated with TMEM107
Meckel syndrome 13
orofaciodigital syndrome XVI

Mouse Phenotypes
abnormal basioccipital bone morphology
basisphenoid bone foramen
small basisphenoid bone
abnormal exoccipital bone morphology
absent presphenoid bone
short presphenoid bone
palatal shelf hypoplasia
cleft palate
Availability Mouse Genotype
Tmem107schlei/Tmem107schlei

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