Ift25 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Ift25
intraflagellar transport 25
MGI:1920188

24 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ift25^{tm1a(EUCOMM)Wtsi}/Ift25⁺ B6JTyr;B6N-Ift25^{tm1a(EUCOMM)Wtsi}/Wtsi	abnormal behavior	J:175295
	increased circulating free fatty acids level	J:175295
	increased circulating glycerol level	J:175295
Ift25^{tm1a(EUCOMM)Wtsi}/Ift25^{tm1a(EUCOMM)Wtsi} B6JTyr;B6N-Ift25^{tm1a(EUCOMM)Wtsi}/Wtsi	preweaning lethality, complete penetrance	J:211773
Ift25^{tm1a(EUCOMM)Wtsi}/Ift25^{tm1a(EUCOMM)Wtsi} involves: C57BL/6J * C57BL/6N	abnormal atrioventricular cushion morphology	J:184749
	abnormal heart size	J:184749
	abnormal neural tube morphology	J:184749
	abnormal sternebra morphology	J:184749
	atrioventricular septal defect	J:184749
	cleft palate	J:184749
	cyanosis	J:184749
	decreased birth body size	J:184749
	double outlet right ventricle	J:184749
	fetal growth retardation	J:184749
	left pulmonary isomerism	J:184749
	micrognathia	J:184749
	neonatal lethality, complete penetrance	J:184749
	omphalocele	J:184749
	overriding aortic valve	J:184749
	polydactyly	J:184749
	preaxial polydactyly	J:184749
	small thoracic cage	J:184749
	unbalanced complete common atrioventricular canal	J:184749
	ventricular septal defect	J:184749
Ift25^{tm1b(EUCOMM)Wtsi}/Ift25^{tm1b(EUCOMM)Wtsi} involves: C57BL/6J * C57BL/6N	abnormal atrioventricular cushion morphology	J:184749
	abnormal heart size	J:184749
	abnormal neural tube morphology	J:184749
	abnormal sternebra morphology	J:184749
	atrioventricular septal defect	J:184749
	cleft palate	J:184749
	cyanosis	J:184749
	decreased birth body size	J:184749
	double outlet right ventricle	J:184749
	fetal growth retardation	J:184749
	left pulmonary isomerism	J:184749
	micrognathia	J:184749
	neonatal lethality, complete penetrance	J:184749
	omphalocele	J:184749
	overriding aortic valve	J:184749
	polydactyly	J:184749
	preaxial polydactyly	J:184749
	small thoracic cage	J:184749
	unbalanced complete common atrioventricular canal	J:184749
	ventricular septal defect	J:184749

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 11/12/2024 MGI 6.24