Urm1 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Urm1
ubiquitin related modifier 1
MGI:1915455

21 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Urm1^em1(IMPC)J/Urm1⁺ C57BL/6NJ-Urm1^em1(IMPC)J/Mmjax	impaired glucose tolerance	J:211773
Urm1^em1(IMPC)J/Urm1⁺ C57BL/6NJ-Urm1^em1(IMPC)J/Mmjax	increased circulating aspartate transaminase level	J:211773
Urm1^em1(IMPC)J/Urm1^em1(IMPC)J C57BL/6NJ-Urm1^em1(IMPC)J/Mmjax	abnormal chorioallantoic fusion	J:374598
	abnormal embryo morphology	J:374598
	abnormal forebrain morphology	J:374598
	abnormal head shape	J:374598
	abnormal heart development	J:374598
	abnormal pharyngeal arch morphology	J:374598
	abnormal placenta development	J:374598
	abnormal placenta labyrinth morphology	J:374598
	abnormal trophoblast layer morphology	J:374598
	decreased embryo size	J:374598
	decreased spongiotrophoblast size	J:374598
	embryonic growth retardation	J:374598
	embryonic lethality during organogenesis, complete penetrance	J:374598
	embryonic lethality prior to tooth bud stage	J:211773
	hemorrhage	J:374598
	incomplete embryo turning	J:374598
	incomplete rostral neuropore closure	J:374598
	kinked neural tube	J:374598
	preweaning lethality, complete penetrance	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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