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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
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Allelic Composition
Genetic Background
Annotated Term Reference
Uhrf2em1Yoz/Uhrf2em1Yoz
FVB/N-Uhrf2em1Yoz
abnormal DNA methylation J:241384
abnormal spatial reference memory J:241384
impaired contextual conditioning behavior J:241384
Uhrf2tm1b(EUCOMM)Wtsi/Uhrf2tm1b(EUCOMM)Wtsi
C57BL/6N-Uhrf2tm1b(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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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory