lg Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

lg
lid gap
MGI:96775

11 phenotypes from 4 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
lg/lg Not Specified	abnormal eye development	J:5056
	abnormal eyelid fusion	J:5056
	eyelids open at birth	J:5056, J:65328
lg^Ml/lg^Ml C3H/Ml	abnormal eyelid development	J:24765
lg^Ml/lg^Ml C3H/Ml	eyelids open at birth	J:24765
lg^St/lg^St involves: L	abnormal eye development	J:27504
	abnormal eye morphology	J:27504
	abnormal eyelid development	J:27504
	anophthalmia	J:27504
	cataract	J:27504
	eyelids open at birth	J:27504
	microphthalmia	J:27504
lg^Stn/lg^Stn Not Specified	abnormal cornea morphology	J:5166
	abnormal eye development	J:5166, J:7160, J:7495, J:8009
	abnormal retina morphology	J:5166
	eyelids open at birth	J:5056
	lens vacuoles	J:5166

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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