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)
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