Cox5b Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Cox5b
cytochrome c oxidase subunit 5B
MGI:88475

9 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Cox5b^{tm2b(EUCOMM)Hmgu}/Cox5b⁺ C57BL/6N-Cox5b^{tm2b(EUCOMM)Hmgu}/Bay	abnormal skin coloration	J:211773
	persistence of hyaloid vascular system	J:211773
	unresponsive to tactile stimuli	J:211773
Cox5b^{tm2b(EUCOMM)Hmgu}/Cox5b^{tm2b(EUCOMM)Hmgu} C57BL/6N-Cox5b^{tm2b(EUCOMM)Hmgu}/Bay	abnormal embryonic autopod plate morphology	J:211773
	abnormal liver size	J:211773
	pale liver	J:211773
	pallor	J:211773
	prenatal lethality prior to heart atrial septation	J:211773
	preweaning lethality, complete penetrance	J:211773

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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