Spryd3 Phenotype Annotations

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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

Allelic Composition Genetic Background	Annotated Term	Reference
Spryd3^{tm1a(EUCOMM)Hmgu}/Spryd3^{tm1a(EUCOMM)Hmgu} C57BL/6N-Spryd3^{tm1a(EUCOMM)Hmgu}/Ieg	abnormal behavior	J:165965
	decreased body weight	J:165965
	hyperactivity	J:165965
	increased circulating alkaline phosphatase level	J:165965
Spryd3^{tm1b(EUCOMM)Hmgu}/Spryd3^{tm1b(EUCOMM)Hmgu} C57BL/6N-Spryd3^{tm1b(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
	cataract	J:211773
	decreased mean corpuscular hemoglobin concentration	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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