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 | Optic atrophy |
Optic disc pallor |
Visual impairment |
Blindness |
Visual loss |
Disease(s) Associated with CLCN7 | |||||
autosomal dominant osteopetrosis 2 | |||||
autosomal recessive osteopetrosis 4 |
Mouse Phenotypes | vision/eye phenotype |
absent photoreceptor inner segment |
absent photoreceptor outer segment |
optic nerve degeneration |
abnormal retina pigment epithelium morphology |
thin retina inner nuclear layer |
thin retina outer nuclear layer |
retina degeneration |
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Availability | Mouse Genotype | ||||||||
Clcn7tm1.1Lex/Clcn7tm1.1Lex | * | ||||||||
Clcn7tm1Tjj/Clcn7tm1Tjj | |||||||||
Clcn7tm2Tjj/Clcn7tm2Tjj | |||||||||
Clcn7tm4.1Tjj/Clcn7tm4.1Tjj | |||||||||
Clcn7tm5.1Tjj/Clcn7tm5.1Tjj | * | ||||||||
Clcn7tm4.1Tjj/Clcn7+ |
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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