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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Nr2f6
nuclear receptor subfamily 2, group F, member 6
MGI:1352453
8 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Nr2f6em1(IMPC)H/Nr2f6em1(IMPC)H
C57BL/6N-Nr2f6em1(IMPC)H/H
abnormal bone structure J:211773
decreased bone mineral content J:211773
Nr2f6tm1Ge/Nr2f6tm1Ge
involves: 129S5/SvEvBrd * C57BL/6J
abnormal circadian behavior J:96328
abnormal locomotor circadian rhythm J:96328
abnormal nociception after inflammation J:96328
abnormal synaptic norepinephrine release J:96328
abnormal thermal nociception J:96328
shortened circadian behavior period J:96328

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
10/29/2024
MGI 6.24
The Jackson Laboratory