Fbxl19 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Fbxl19
F-box and leucine-rich repeat protein 19
MGI:3039600

17 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fbxl19^tm1.2Hko/Fbxl19^tm1.2Hko involves: 129 * C57BL/6	abnormal cardiac mesenchyme morphology	J:316372
	abnormal first pharyngeal arch morphology	J:316372
	abnormal head mesenchyme morphology	J:316372
	decreased body length	J:316372
	delayed head development	J:316372
	embryonic growth retardation	J:316372
	prenatal lethality, complete penetrance	J:316372
	small limb buds	J:316372
Fbxl19^{tm1b(EUCOMM)Wtsi}/Fbxl19⁺ C57BL/6N-Fbxl19^{tm1b(EUCOMM)Wtsi}/Nju	decreased circulating glucose level	J:211773
	decreased circulating total protein level	J:211773
	decreased lymphocyte cell number	J:211773
	increased basophil cell number	J:211773
	increased eosinophil cell number	J:211773
	increased leukocyte cell number	J:211773
	increased mean platelet volume	J:211773
	increased monocyte cell number	J:211773
	increased neutrophil cell number	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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