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Symbol
Name
ID

Rpgrip1l
Rpgrip1-like
MGI:1920563

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes

Abnormality of retinal pigmentation

Bone spicule pigmentation of the retina

Retinal dystrophy

Rod-cone dystrophy

Perifoveal hypoautofluorescence

Microphthalmia

Nystagmus

Oculomotor apraxia

High myopia

Color vision defect

Nyctalopia

Photophobia

Reduced visual acuity

Constriction of peripheral visual field

Ring scotoma

Ptosis

Disease(s) Associated with RPGRIP1L

Joubert syndrome 7

Meckel syndrome 5

nephronophthisis

retinitis pigmentosa 3

Mouse Phenotypes		abnormal eye muscle morphology	absent optic chiasm	abnormal optic cup morphology	abnormal optic stalk morphology	microphthalmia	anophthalmia
Availability	Mouse Genotype	abnormal eye muscle morphology	absent optic chiasm	abnormal optic cup morphology	abnormal optic stalk morphology	microphthalmia	anophthalmia
	Rpgrip1l^{tm1a(EUCOMM)Wtsi}/Rpgrip1l^{tm1a(EUCOMM)Wtsi}
	Rpgrip1l^tm1Urt/Rpgrip1l^tm1Urt

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/23/2024 MGI 6.23