Eif3f Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Eif3f
eukaryotic translation initiation factor 3, subunit F
MGI:1913335

30 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Eif3f^{em1(IMPC)Hmgu}/Eif3f⁺ C57BL/6N-Eif3f^{em1(IMPC)Hmgu}/Ieg	abnormal coat/hair pigmentation	J:211773
	abnormal cornea morphology	J:211773
	abnormal eyelid morphology	J:211773
	abnormal iris morphology	J:211773
	abnormal lens morphology	J:211773
	abnormal optic disk morphology	J:211773
	abnormal placement of pupils	J:211773
	abnormal retina blood vessel morphology	J:211773
	abnormal retina morphology	J:211773
	abnormal retina vasculature morphology	J:211773
	cataract	J:211773
	cornea deposits	J:211773
	cornea opacity	J:211773
	eyelids fail to open	J:211773
	fused cornea and lens	J:211773
	iris synechia	J:211773
	irregularly shaped pupil	J:211773
	narrow eye opening	J:211773
	persistence of hyaloid vascular system	J:211773
	sclerocornea	J:211773
Eif3f^{em1(IMPC)Hmgu}/Eif3f^{em1(IMPC)Hmgu} C57BL/6N-Eif3f^{em1(IMPC)Hmgu}/Ieg	preweaning lethality, complete penetrance	J:211773
Eif3f^{tm1(KOMP)Vlcg}/Eif3f⁺ B6J.B6N-Eif3f^{tm1(KOMP)Vlcg}	abnormal muscle physiology	J:294674
	abnormal translation	J:294674
	decreased lean body mass	J:294674
	decreased skeletal muscle fiber size	J:294674
	decreased skeletal muscle mass	J:294674
	increased susceptibility to induced muscular atrophy	J:294674
	prenatal lethality, incomplete penetrance	J:294674
Eif3f^{tm1(KOMP)Vlcg}/Eif3f^{tm1(KOMP)Vlcg} B6J.B6N-Eif3f^{tm1(KOMP)Vlcg}	embryonic lethality, complete penetrance	J:294674
	empty decidua capsularis	J:294674

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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