Ncor2 Phenotype Annotations - Multigenic Genotypes

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Ncor2
nuclear receptor co-repressor 2
MGI:1337080

4 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Foxp1^{Gt(S17-4A1)Sor}/Foxp1⁺ Ncor2^tm1Rsd/Ncor2⁺ involves: 129/Sv * 129S4/SvJaeSor	prenatal lethality, incomplete penetrance	J:132982
	thin myocardium	J:132982
	ventricular septal defect	J:132982
Ncor1^tm1Rsd/Ncor1⁺ Ncor2^tm1Rsd/Ncor2⁺ involves: 129/Sv * 129S1/Sv * 129X1/SvJ	abnormal neuron differentiation	J:127720

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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