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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Ccdc66
coiled-coil domain containing 66
MGI:2443639
13 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Ccdc66em1(IMPC)Mbp/Ccdc66em1(IMPC)Mbp
C57BL/6NCrl-Ccdc66em1(IMPC)Mbp/MbpMmucd 		decreased mean corpuscular hemoglobin concentration J:211773
impaired glucose tolerance J:211773
increased hematocrit J:211773
Ccdc66Gt(E021F10)Wrst/Ccdc66Gt(E021F10)Wrst
involves: 129P2/OlaHsd * C57BL/6N 		abnormal cone electrophysiology J:174954
abnormal photoreceptor inner segment morphology J:174954
abnormal photoreceptor outer segment morphology J:174954
abnormal retina photoreceptor layer morphology J:174954
abnormal retina rod cell morphology J:174954
abnormal rod electrophysiology J:174954
retina cone cell degeneration J:174954
retina photoreceptor degeneration J:174954
retina rod cell degeneration J:174954
thin retina outer nuclear layer J:174954
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
11/12/2024
MGI 6.24 		The Jackson Laboratory