About   Help   FAQ
Symbol
Name
ID 		Rnf168
ring finger protein 168
MGI:1917488
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Conjunctival telangiectasia
Disease(s) Associated with RNF168
RIDDLE syndrome

Mouse Phenotypes
abnormal retina vasculature morphology
abnormal retina blood vessel morphology
abnormal optic disk morphology
abnormal eye morphology
abnormal cornea morphology
corneal opacity
fused cornea and lens
abnormal lens morphology
cataract
microphthalmia
narrow eye opening
eyelids fail to open
abnormal retina morphology
anophthalmia
Availability Mouse Genotype
Rnf168em1(IMPC)H/Rnf168em1(IMPC)H
Rnf168tm2b(EUCOMM)Hmgu/Rnf168tm2b(EUCOMM)Hmgu
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
04/16/2024
MGI 6.23 		The Jackson Laboratory