Nr2c1 Phenotype Annotations

About Help FAQ

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Nr2c1
nuclear receptor subfamily 2, group C, member 1
MGI:1352465

2 phenotypes from 1 allele in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Nr2c1^tm1Chc/Nr2c1^tm1Chc involves: 129S5/SvEvBrd	abnormal hemoglobin	J:121628
Nr2c1^tm1Chc/Nr2c1^tm1Chc involves: 129S5/SvEvBrd * C57BL/6	no abnormal phenotype detected	J:77023

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/16/2024 MGI 6.23