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Symbol
Name
ID

Bbs7
Bardet-Biedl syndrome 7
MGI:1918742

Phenotype annotations related to vision/eye

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes

Astigmatism

Cataract

Retinal dystrophy

Cone/cone-rod dystrophy

Rod-cone dystrophy

Deeply set eye

Hypertelorism

Abnormal electroretinogram

Strabismus

Nystagmus

Color vision defect

Nyctalopia

Photophobia

Reduced visual acuity

Blindness

Disease(s) Associated with BBS7

Bardet-Biedl syndrome

Bardet-Biedl syndrome 7

Mouse Phenotypes		vision/eye phenotype	photoreceptor inner segment degeneration	photoreceptor outer segment degeneration	abnormal lens morphology	retina outer nuclear layer degeneration	retina degeneration
Availability	Mouse Genotype	vision/eye phenotype	photoreceptor inner segment degeneration	photoreceptor outer segment degeneration	abnormal lens morphology	retina outer nuclear layer degeneration	retina degeneration
	Bbs7^tm1Vcs/Bbs7^tm1Vcs	*
	Bbs7^{tm1b(EUCOMM)Wtsi}/Bbs7⁺

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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