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Symbol
Name
ID
Tmem107
transmembrane protein 107
MGI:1914160
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
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
camptomelia
short sternum
split sternum
rib bifurcation
delayed intramembranous bone ossification
Availability Mouse Genotype
Tmem107schlei/Tmem107schlei

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/09/2019
MGI 6.13
The Jackson Laboratory