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Symbol
Name
ID
Tmem67
transmembrane protein 67
MGI:1923928
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Cleft palate
Chorioretinal coloboma
Dandy-Walker malformation
Encephalocele
Disease(s) Associated with TMEM67
Joubert syndrome 6
Meckel syndrome 3

Mouse Phenotypes
abnormal posterior cranial fossa morphology
mandible hypoplasia
Availability Mouse Genotype
Tmem67tm1Dgen/Tmem67tm1Dgen

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Funding Information
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last database update
02/12/2019
MGI 6.13
The Jackson Laboratory