Symbol Name ID |
Clcn7
chloride channel, voltage-sensitive 7 MGI:1347048 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal leukocyte morphology |
Mandibular osteomyelitis |
Tooth abscess |
Splenomegaly |
Osteomyelitis |
Disease(s) Associated with CLCN7 | |||||
autosomal dominant osteopetrosis 2 | |||||
autosomal recessive osteopetrosis 4 |
Mouse Phenotypes | increased osteoclast cell number |
microgliosis |
abnormal osteoclast morphology |
abnormal osteoclast physiology |
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Availability | Mouse Genotype | ||||
Clcn7tm1.1Lex/Clcn7tm1.1Lex | |||||
Clcn7tm1Tjj/Clcn7tm1Tjj | |||||
Clcn7tm2Tjj/Clcn7tm2Tjj | |||||
Clcn7tm4.1Tjj/Clcn7tm4.1Tjj | |||||
Clcn7tm5.1Tjj/Clcn7tm5.1Tjj | |||||
Clcn7tm1.1Mawa/Clcn7+ | |||||
Clcn7tm1.1Teti/Clcn7+ | |||||
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 09/03/2024 MGI 6.24 |
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