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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
Micrognathia
Retrognathia
Occipital encephalocele
Hamartoma of tongue
Depressed nasal bridge
Short palpebral fissure
Disease(s) Associated with TMEM107
Meckel syndrome 13
orofaciodigital syndrome XVI

Mouse Phenotypes
abnormal craniofacial morphology
abnormal cranium morphology
abnormal basioccipital bone morphology
abnormal basisphenoid bone morphology
basisphenoid bone foramen
impaired ossification of basisphenoid bone
small basisphenoid bone
short Meckel's cartilage
abnormal cranial cartilage development
small frontal bone
abnormal exoccipital bone morphology
small parietal bone
absent presphenoid bone
short presphenoid bone
abnormal mandible morphology
short mandible
abnormal maxilla morphology
decreased maxillary shelf size
abnormal premaxilla morphology
small maxilla
absent nasal bone
small nasal bone
abnormal palatine bone morphology
small zygomatic bone
abnormal palatal mesenchymal cell proliferation
abnormal palatal shelf morphology
abnormal palatal shelf bone ossification
abnormal palatal shelf elevation
palatal shelves fail to meet at midline
palatal shelf hypoplasia
abnormal facial morphology
cleft upper lip
unilateral cleft upper lip
abnormal palatal rugae morphology
cleft secondary palate
cleft palate
abnormal tongue morphology
abnormal tongue position
decreased tongue size
abnormal nasal septum cartilage morphology
abnormal vomeronasal cartilage morphology
abnormal vomeronasal organ morphology
large nasal septum
thick nasal septum
abnormal snout morphology
broad snout
short snout
abnormal head shape
Availability Mouse Genotype
Tmem107schlei/Tmem107schlei
Tmem107tm1Lex/Tmem107tm1Lex

Contributing Projects:
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
03/19/2024
MGI 6.23
The Jackson Laboratory