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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
Biparietal narrowing
Retrognathia
Dandy-Walker malformation
Macrocephaly
Encephalocele
Occipital encephalocele
Long face
Round face
Abnormal oral cavity morphology
Long philtrum
Cleft palate
High palate
Wide mouth
Microdontia
Hypodontia
Dental crowding
Orofacial cleft
Anteverted nares
Depressed nasal bridge
Prominent nasal bridge
Abnormality of the sense of smell
Rhinitis
Highly arched eyebrow
Medial flaring of the eyebrow
Downslanted palpebral fissures
Disease(s) Associated with TMEM67
Bardet-Biedl syndrome
COACH syndrome
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 Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory