Sco2 Phenotype Annotations

About Help FAQ

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Sco2
SCO2 cytochrome c oxidase assembly protein
MGI:3818630

8 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Sco2^tm1.1Easc/Sco2^tm1.1Easc 129X1/SvJ-Sco2^tm1.1Easc	abnormal embryonic tissue morphology	J:155116
Sco2^tm1.1Easc/Sco2^tm1.1Easc 129X1/SvJ-Sco2^tm1.1Easc	embryonic lethality between implantation and placentation, complete penetrance	J:155116
Sco2^tm1.1Easc/Sco2^tm2.1Easc 129X1/SvJ-Sco2^tm1.1Easc/Sco2^tm2.1Easc	abnormal copper level	J:155116
	abnormal locomotor behavior	J:176080
	abnormal mitochondrial ATP synthesis coupled electron transport	J:155116
	impaired exercise endurance	J:155116
	increased liver copper level	J:155116
	muscle weakness	J:155116
Sco2^tm2.1Easc/Sco2^tm2.1Easc 129X1/SvJ-Sco2^tm2.1Easc	abnormal copper level	J:155116
	abnormal mitochondrial ATP synthesis coupled electron transport	J:155116
	muscle weakness	J:155116

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