Smarcd2 Phenotype Annotations

About Help FAQ

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Smarcd2
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 2
MGI:1933621

5 phenotypes from 1 allele in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Smarcd2^{tm1.1(KOMP)Vlcg}/Smarcd2⁺ C57BL/6N-Smarcd2^{tm1.1(KOMP)Vlcg}/Ucd	decreased prepulse inhibition	J:211773
	edema	J:211773
	increased mean corpuscular volume	J:211773
Smarcd2^{tm1.1(KOMP)Vlcg}/Smarcd2^{tm1.1(KOMP)Vlcg} C57BL/6N-Smarcd2^{tm1.1(KOMP)Vlcg}/Ucd	edema	J:211773
	preweaning lethality, incomplete penetrance	J:211773
Smarcd2^{tm1.1(KOMP)Vlcg}/Smarcd2^{tm1.1(KOMP)Vlcg} involves: C57BL/6NTac	lethality, complete penetrance	J:255772

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