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Symbol
Name
ID
Clcn7
chloride channel, voltage-sensitive 7
MGI:1347048
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Facial palsy
Facial paralysis
Frontal bossing
Carious teeth
Mandibular osteomyelitis
Macrocephaly
Disease(s) Associated with CLCN7
autosomal dominant osteopetrosis 2
autosomal recessive osteopetrosis 4

Mouse Phenotypes
small cranium
abnormal tooth eruption
failure of tooth eruption
Availability Mouse Genotype
Clcn7tm1.1Teti/Clcn7tm1.1Teti
Clcn7tm1Tjj/Clcn7tm1Tjj
Clcn7tm2Tjj/Clcn7tm2Tjj
Clcn7tm4.1Tjj/Clcn7tm4.1Tjj

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
12/04/2018
MGI 6.13
The Jackson Laboratory