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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Rd3
retinal degeneration 3
MGI:1921273
13 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Rd3em1(IMPC)Bay/Rd3em1(IMPC)Bay
C57BL/6N-Rd3em1(IMPC)Bay/BayMmucd
abnormal eye anterior chamber depth J:211773
abnormal retina inner nuclear layer morphology J:211773
abnormal retina morphology J:211773
abnormal retina outer nuclear layer morphology J:211773
decreased mean corpuscular hemoglobin concentration J:211773
decreased total retina thickness J:211773
increased cornea thickness J:211773
increased hematocrit J:211773
Rd3rd3/Rd3rd3
RBF/DnJ-Rd3rd3
abnormal eye electrophysiology J:4367
abnormal retina photoreceptor layer morphology J:4367
absent retina rod cells J:4367
retina photoreceptor degeneration J:4367
thin retina outer nuclear layer J:4367

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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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory