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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		rd21
retinal degeneration 21
MGI:5906364
10 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background		 Annotated Term Reference
rd21/rd21
Not Specified 		abnormal cone electrophysiology J:242762
abnormal eye electrophysiology J:242762
abnormal retina vasculature morphology J:242762
abnormal rod electrophysiology J:242762
absent visual evoked potential J:242762
retina cone cell degeneration J:242762
retina degeneration J:242762
retina detachment J:242762
retina photoreceptor degeneration J:242762
retina rod cell degeneration J:242762
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
05/07/2024
MGI 6.23 		The Jackson Laboratory