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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
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Allelic Composition
Genetic Background		 Annotated Term Reference
Sco1tm1c(KOMP)Wtsi/Sco1tm1c(KOMP)Wtsi
Speer6-ps1Tg(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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory