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Symbol
Name
ID

Rho
rhodopsin
MGI:97914

Phenotype annotations related to vision/eye

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

Human Phenotypes

Abnormal retinal vascular morphology

Attenuation of retinal blood vessels

Keratoconus

Cataract

Posterior subcapsular cataract

Optic atrophy

Optic disc pallor

Abnormality of retinal pigmentation

Pigmentary retinopathy

Bone spicule pigmentation of the retina

Retinal degeneration

Retinal atrophy

Congenital stationary night blindness

Fundus albipunctatus

Rod-cone dystrophy

Retinal flecks

Abnormal electroretinogram

Decreased light- and dark-adapted electroretinogram amplitude

Nystagmus

Ophthalmoplegia

Nyctalopia

Progressive night blindness

Photophobia

Photopsia

Visual impairment

Reduced visual acuity

Blindness

Visual field defect

Peripheral visual field loss

Glaucoma

Disease(s) Associated with RHO

congenital stationary night blindness autosomal dominant 1

fundus albipunctatus

retinitis pigmentosa

retinitis pigmentosa 4

Mouse Phenotypes

vision/eye phenotype

abnormal retina vasculature morphology

increased retina apoptosis

photosensitivity

decreased retina photoreceptor cell number

decreased retina rod cell number

abnormal retina photoreceptor morphology

disorganized photoreceptor inner segment

abnormal photoreceptor outer segment morphology

absent photoreceptor outer segment

short photoreceptor outer segment

short retina rod cell outer segment

disorganized photoreceptor outer segment

abnormal retina cone cell morphology

retina rod cell degeneration

retina photoreceptor degeneration

abnormal retina pigment epithelium morphology

abnormal retina pigmentation

abnormal eye development

abnormal ocular fundus morphology

abnormal retina morphology

abnormal retina layer morphology

abnormal retina inner nuclear layer morphology

thin retina inner nuclear layer

thin retina outer nuclear layer

disorganized retina outer nuclear layer

retina outer nuclear layer degeneration

thin retina outer plexiform layer

abnormal retina photoreceptor layer morphology

disorganized retina layers

increased susceptibility to age-related retinal degeneration

decreased total retina thickness

retina degeneration

retina detachment

abnormal a-wave shape

decreased a-wave amplitude

decreased b-wave amplitude

absent b-wave

abnormal eye electrophysiology

abnormal cone electrophysiology

abnormal rod electrophysiology

abnormal vision

delayed dark adaptation

Availability

Mouse Genotype

Rho^Noerg1/Rho^Noerg1

Rho^R3/Rho^R3

Rho^{tm1.1(RHO*)Akgr}/Rho^{tm1.1(RHO*)Akgr}

Rho^tm1.1Kpal/Rho^tm1.1Kpal

Rho^tm1Jlem/Rho^tm1Jlem

Rho^tm1Phm/Rho^tm1Phm

Rho^tm2.1Kpal/Rho^tm2.1Kpal

*

Rho^tm2Jlem/Rho^tm2Jlem

Rho^Tvrm144/Rho^Tvrm144

Rho^Tvrm334/Rho^Tvrm334

Rho^Noerg1/Rho⁺

Rho^R3/Rho⁺

Rho^R3/Rho^tm1Jlem

Rho^{tm1.1(RHO*)Akgr}/Rho⁺

Rho^tm1.1Eye/Rho⁺

Rho^tm1.1Kpal/Rho⁺

Rho^tm1Jlem/Rho⁺

Rho^tm1Phm/Rho⁺

Rho^tm2.1Kpal/Rho⁺

Rho^Tvrm1/Rho⁺

Rho^Tvrm4/Rho⁺

Rho^Tvrm144/Rho⁺

Rho^Tvrm334/Rho⁺

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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