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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	Optic disc pallor	Visual impairment	Blindness	Visual loss
Disease(s) Associated with CLCN7	Optic atrophy	Optic disc pallor	Visual impairment	Blindness	Visual loss
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
Availability	Mouse Genotype	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
	Clcn7^tm1.1Lex/Clcn7^tm1.1Lex	*
	Clcn7^tm1Tjj/Clcn7^tm1Tjj
	Clcn7^tm2Tjj/Clcn7^tm2Tjj
	Clcn7^tm4.1Tjj/Clcn7^tm4.1Tjj
	Clcn7^tm5.1Tjj/Clcn7^tm5.1Tjj	*
	Clcn7^tm4.1Tjj/Clcn7⁺

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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