Ubr2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Ubr2
ubiquitin protein ligase E3 component n-recognin 2
MGI:1861099

17 phenotypes from 2 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ubr2^{tm1e.1(KOMP)Mbp}/Ubr2⁺ C57BL/6N-Ubr2^{tm1e.1(KOMP)Mbp}/Tcp	abnormal liver morphology	J:211773
	hemorrhage	J:211773
	spina bifida	J:211773
Ubr2^{tm1e.1(KOMP)Mbp}/Ubr2^{tm1e.1(KOMP)Mbp} C57BL/6N-Ubr2^{tm1e.1(KOMP)Mbp}/Tcp	hemorrhage	J:211773
	preweaning lethality, complete penetrance	J:211773
	preweaning lethality, incomplete penetrance	J:211773
	spina bifida	J:211773
Ubr2^tm1Ytkw/Ubr2^tm1Ytkw involves: 129S1/Sv	prenatal lethality, incomplete penetrance	J:86438
Ubr2^tm1Ytkw/Ubr2^tm1Ytkw involves: 129S1/Sv	testis degeneration	J:86438
Ubr2^tm1Ytkw/Ubr2^tm1Ytkw involves: 129S1/Sv * C57BL/6	abnormal embryonic tissue morphology	J:86438
	abnormal embryonic tissue physiology	J:86438
	abnormal fertility/fecundity	J:86438
	abnormal gametogenesis	J:86438
	arrest of male meiosis	J:86438
	increased embryonic tissue cell apoptosis	J:86438
	male infertility	J:86438
	oligozoospermia	J:86438
	postnatal growth retardation	J:86438
	prenatal lethality, incomplete penetrance	J:86438
	reduced female fertility	J:86438
	testis degeneration	J:86438
Ubr2^tm1Ytkw/Ubr2^tm1Ytkw involves: 129S1/Sv * CD-1	prenatal lethality, incomplete penetrance	J:86438
Ubr2^tm1Ytkw/Ubr2^tm1Ytkw involves: 129S1/Sv * CD-1	testis degeneration	J:86438

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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