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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
Mandibular osteomyelitis
Macrocephaly
Frontal bossing
Facial palsy
Facial paralysis
Abnormality of the dentition
Carious teeth
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
Clcn7tm1.1Mawa/Clcn7tm1.1Mawa
Clcn7tm1.1Teti/Clcn7tm1.1Teti
Clcn7tm1Tjj/Clcn7tm1Tjj
Clcn7tm2Tjj/Clcn7tm2Tjj
Clcn7tm4.1Tjj/Clcn7tm4.1Tjj
Clcn7tm5.1Tjj/Clcn7tm5.1Tjj
Clcn7tm1.1Mawa/Clcn7tm1.1Mjec

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
10/15/2019
MGI 6.14
The Jackson Laboratory