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Symbol
Name
ID
Clcn7
chloride channel, voltage-sensitive 7
MGI:1347048
Phenotype annotations related to vision/eye
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Optic atrophy
Blindness
Visual loss
Disease(s) Associated with CLCN7
autosomal dominant osteopetrosis 2

Mouse Phenotypes
vision/eye phenotype
absent photoreceptor inner segment
absent photoreceptor outer segment
optic nerve degeneration
abnormal retinal pigment epithelium morphology
thin retinal inner nuclear layer
thin retinal outer nuclear layer
retinal degeneration
Availability Mouse Genotype
Clcn7tm1.1Lex/Clcn7tm1.1Lex *
Clcn7tm1Tjj/Clcn7tm1Tjj
Clcn7tm2Tjj/Clcn7tm2Tjj
Clcn7tm4.1Tjj/Clcn7tm4.1Tjj
Clcn7tm4.1Tjj/Clcn7+

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/11/2018
MGI 6.13
The Jackson Laboratory