Uhrf2 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Uhrf2
ubiquitin-like, containing PHD and RING finger domains 2
MGI:1923718

17 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Uhrf2^em1Yoz/Uhrf2^em1Yoz FVB/N-Uhrf2^em1Yoz	abnormal DNA methylation	J:241384
	abnormal spatial reference memory	J:241384
	impaired contextual conditioning behavior	J:241384
Uhrf2^{tm1b(EUCOMM)Wtsi}/Uhrf2^{tm1b(EUCOMM)Wtsi} C57BL/6N-Uhrf2^{tm1b(EUCOMM)Wtsi}/Tcp	abnormal bone structure	J:211773
	decreased body length	J:211773
	decreased bone mineral content	J:211773
	decreased bone mineral density	J:211773
	decreased heart rate	J:211773
	decreased lean body mass	J:211773
	female infertility	J:211773
	hyperactivity	J:211773
	increased circulating alkaline phosphatase level	J:211773
	increased leukocyte cell number	J:211773
	increased lymphocyte cell number	J:211773
	increased total body fat amount	J:211773
	preweaning lethality, incomplete penetrance	J:211773
	prolonged RR interval	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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