Vipr1 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Vipr1
vasoactive intestinal peptide receptor 1
MGI:109272

20 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Vipr1^tm1Dgen/Vipr1^tm1Dgen involves: 129P2/OlaHsd * C57BL/6J	abnormal gait	J:82809
	ataxia	J:82809
	decreased locomotor activity	J:82809
	hunched posture	J:82809
	impaired coordination	J:82809
	preweaning lethality, incomplete penetrance	J:82809
Vipr1^tm1Msod/Vipr1^tm1Msod B6.129-Vipr1^tm1Msod	abnormal enterocyte proliferation	J:177616
	abnormal exocrine pancreas morphology	J:177616
	abnormal glucose homeostasis	J:177616
	abnormal intestine morphology	J:177616
	decreased body weight	J:177616
	disorganized pancreatic islets	J:177616
	enlarged cecum	J:177616
	hypoglycemia	J:177616
	impaired glucose tolerance	J:177616
	increased insulin sensitivity	J:177616
	intestinal obstruction	J:177616
	lethality at weaning, incomplete penetrance	J:177616
	postnatal growth retardation	J:177616
	preweaning lethality, incomplete penetrance	J:177616
	small intestine hemorrhage	J:177616

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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