Symbol Name ID |
Clcn7
chloride channel, voltage-sensitive 7 MGI:1347048 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Splenomegaly |
Hepatomegaly |
Short stature |
Growth delay |
Disease(s) Associated with CLCN7 | ||||
autosomal dominant osteopetrosis 2 | ||||
autosomal recessive osteopetrosis 4 |
Mouse Phenotypes | abnormal tooth eruption |
failure of tooth eruption |
growth/size/body region phenotype |
decreased body weight |
increased body weight |
abnormal head morphology |
decreased body length |
decreased body size |
postnatal growth retardation |
|
Availability | Mouse Genotype | |||||||||
Clcn7tm1.1Aros/Clcn7tm1.1Aros | ||||||||||
Clcn7tm1.1Lex/Clcn7tm1.1Lex | ||||||||||
Clcn7tm1.1Mawa/Clcn7tm1.1Mawa | ||||||||||
Clcn7tm1.1Teti/Clcn7tm1.1Teti | ||||||||||
Clcn7tm1Tjj/Clcn7tm1Tjj | ||||||||||
Clcn7tm2.1Mjec/Clcn7tm2.1Mjec | ||||||||||
Clcn7tm2Tjj/Clcn7tm2Tjj | ||||||||||
Clcn7tm4.1Tjj/Clcn7tm4.1Tjj | ||||||||||
Clcn7tm5.1Tjj/Clcn7tm5.1Tjj | ||||||||||
Clcn7tm1.1Mawa/Clcn7tm1.1Mjec | ||||||||||
Clcn7tm3.1Tjj/Clcn7tm3.1Tjj Emx1tm1.1(cre)Ito/Emx1+ (conditional) |
* |
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 04/30/2024 MGI 6.23 |
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