Fgf15 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Fgf15
fibroblast growth factor 15
MGI:1096383

21 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fgf15^{tm1.1(KOMP)Vlcg}/Fgf15⁺ C57BL/6N-Fgf15^{tm1.1(KOMP)Vlcg}/MbpMmucd	abnormal brain morphology	J:211773
	hydrocephaly	J:211773
Fgf15^{tm1.1(KOMP)Vlcg}/Fgf15^{tm1.1(KOMP)Vlcg} C57BL/6N-Fgf15^{tm1.1(KOMP)Vlcg}/MbpMmucd	preweaning lethality, complete penetrance	J:211773
Fgf15^{tm1.1(KOMP)Vlcg}/Fgf15^{tm1.1(KOMP)Vlcg} C57BL/6N-Fgf15^{tm1.1(KOMP)Vlcg}/Ucd	abnormal embryo size	J:211773
	abnormal heart morphology	J:211773
	abnormal placenta size	J:211773
	edema	J:211773
Fgf15^tm1Sms/Fgf15⁺ involves: 129S1/Sv * 129X1/SvJ * C57BL/6	muscular ventricular septal defect	J:97317
	overriding aortic valve	J:97317
	perimembraneous ventricular septal defect	J:97317
	postnatal lethality	J:97317
	ventricular septal defect	J:97317
Fgf15^tm1Sms/Fgf15^tm1Sms involves: 129S1/Sv * 129X1/SvJ * C57BL/6	aberrant origin of the right subclavian artery	J:97317
	abnormal aorta morphology	J:97317
	abnormal cardiac outflow tract development	J:97317
	abnormal interventricular septum morphology	J:97317
	atrial septal defect	J:97317
	atrioventricular septal defect	J:97317
	double outlet right ventricle	J:97317
	normal hearing/vestibular/ear phenotype	J:90407
	lethality throughout fetal growth and development, incomplete penetrance	J:97317
	muscular ventricular septal defect	J:97317
	overriding aortic valve	J:97317
	perimembraneous ventricular septal defect	J:97317
	postnatal lethality	J:97317
	ventricular septal defect	J:97317

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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