Sco1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Sco1
SCO1 cytochrome c oxidase assembly protein
MGI:106362

17 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Sco1^{tm1c(KOMP)Wtsi}/Sco1^{tm1c(KOMP)Wtsi} Speer6-ps1^{Tg(Alb-cre)21Mgn}/Speer6-ps1⁺ involves: C57BL/6 * C57BL/6N * DBA	abnormal liver morphology	J:222036
	abnormal mitochondrial physiology	J:222036
	decreased body size	J:222036
	decreased kidney copper level	J:222036
	decreased leukocyte cell number	J:222036
	decreased liver copper level	J:222036
	decreased spleen white pulp amount	J:222036
	normal hematopoietic system phenotype	J:222036
	hepatic steatosis	J:222036
	increased liver cholesterol level	J:222036
	increased liver iron level	J:222036
	increased liver triglyceride level	J:222036
	increased mitochondrial number	J:222036
	increased spleen iron level	J:222036
	premature death	J:222036
	spleen atrophy	J:222036
	weight loss	J:222036

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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