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Symbol
Name
ID
Clcn7
chloride channel, voltage-sensitive 7
MGI:1347048
Phenotype annotations related to growth/size/body
*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)
*

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
04/30/2024
MGI 6.23
The Jackson Laboratory