Wrnip1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Wrnip1
Werner helicase interacting protein 1
MGI:1926153

9 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Wrnip1^{tm1a(EUCOMM)Wtsi}/Wrnip1^{tm1a(EUCOMM)Wtsi} C57BL/6N-Wrnip1^{tm1a(EUCOMM)Wtsi}/Cnrm	abnormal behavior	J:165965
	abnormal response to tactile stimuli	J:165965
	decreased circulating triglyceride level	J:165965
	decreased T cell number	J:165965
Wrnip1^{tm1b(EUCOMM)Wtsi}/Wrnip1^{tm1b(EUCOMM)Wtsi} C57BL/6N-Wrnip1^{tm1b(EUCOMM)Wtsi}/Ieg	abnormal retina morphology	J:211773
	abnormal seminal vesicle morphology	J:211773
	decreased locomotor activity	J:211773
	decreased total retina thickness	J:211773
	enlarged cecum	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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