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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Spryd3
SPRY domain containing 3
MGI:2446175
15 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Spryd3tm1a(EUCOMM)Hmgu/Spryd3tm1a(EUCOMM)Hmgu
C57BL/6N-Spryd3tm1a(EUCOMM)Hmgu/Ieg 		abnormal behavior J:165965
decreased body weight J:165965
hyperactivity J:165965
increased circulating alkaline phosphatase level J:165965
Spryd3tm1b(EUCOMM)Hmgu/Spryd3tm1b(EUCOMM)Hmgu
C57BL/6N-Spryd3tm1b(EUCOMM)Hmgu/Ieg 		abnormal lens morphology J:211773
abnormal retina blood vessel morphology J:211773
abnormal retina morphology J:211773
abnormal retina vasculature morphology J:211773
abnormal vitreous body morphology J:211773
cataract J:211773
increased circulating alkaline phosphatase level J:211773
increased circulating cholesterol level J:211773
increased circulating creatinine level J:211773
increased circulating HDL cholesterol level J:211773
increased circulating insulin level J:211773
increased startle reflex J:211773
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
11/19/2024
MGI 6.24 		The Jackson Laboratory