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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		rd22
retinal degeneration 22
MGI:6794091
12 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background		 Annotated Term Reference
rd22/rd22
B6.Cg-rd22/BocJ 		abnormal cone electrophysiology J:347903
abnormal eye electrophysiology J:347903
abnormal eye physiology J:347903
abnormal retina blood vessel morphology J:347903
abnormal retina cone cell morphology J:347903
abnormal retina rod cell inner segment morphology J:347903
abnormal retina rod cell morphology J:347903
abnormal rod electrophysiology J:347903
normal reproductive system phenotype J:347903
retina cone cell degeneration J:347903
retina degeneration J:347903
retina rod cell degeneration J:347903
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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory