Symbol
Name
ID

Sag
S-antigen, retina and pineal gland (arrestin)
MGI:98227

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

Posterior subcapsular cataract

Chorioretinal atrophy

Optic atrophy

Optic disc pallor

Abnormality of retinal pigmentation

Pigmentary retinopathy

Bone spicule pigmentation of the retina

Retinal degeneration

Congenital stationary night blindness

Rod-cone dystrophy

Mizuo phenomenon

Abnormal electroretinogram

Decreased light- and dark-adapted electroretinogram amplitude

Nystagmus

Ophthalmoplegia

Nyctalopia

Progressive night blindness

Photophobia

Photopsia

Visual impairment

Blindness

Peripheral visual field loss

Glaucoma

Disease(s) Associated with SAG

Oguchi disease-1

retinitis pigmentosa

retinitis pigmentosa 47

Mouse Phenotypes		vision/eye phenotype	abnormal retina rod cell outer segment morphology	iris synechia	abnormal rod electrophysiology
Availability	Mouse Genotype	vision/eye phenotype	abnormal retina rod cell outer segment morphology	iris synechia	abnormal rod electrophysiology
	Sag^{tm1a(EUCOMM)Wtsi}/Sag^{tm1a(EUCOMM)Wtsi}
	Sag^tm1Jnc/Sag^tm1Jnc	*

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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