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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	Micrognathia	Retrognathia	Occipital encephalocele	Postaxial hand polydactyly	Postaxial foot polydactyly	Flexion contracture
Disease(s) Associated with TMEM107	Micrognathia	Retrognathia	Occipital encephalocele	Postaxial hand polydactyly	Postaxial foot polydactyly	Flexion contracture
Meckel syndrome 13
orofaciodigital syndrome XVI

Mouse Phenotypes

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 nasal septum cartilage morphology

abnormal vomeronasal cartilage morphology

camptomelia

short sternum

split sternum

rib bifurcation

abnormal intramembranous bone ossification

delayed intramembranous bone ossification

Availability

Mouse Genotype

Tmem107^schlei/Tmem107^schlei

Tmem107^tm1Lex/Tmem107^tm1Lex

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/30/2024 MGI 6.23