Gje1 Phenotype Annotations

About Help FAQ

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Gje1
gap junction protein, epsilon 1
MGI:1923993

12 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Gje1^Mhdaaey12/Gje1⁺ C3HeB/FeJ-Gje1^Mhdaaey12/Ieg	microphthalmia	J:86685
Gje1^Mhdaaey12/Gje1⁺ involves: C3HeB/FeJ	abnormal lens fiber morphology	J:136139
	corneal opacity	J:136139
	increased cornea thickness	J:136139
	microphthalmia	J:136139
	polar cataract	J:136139
	small lens	J:136139
Gje1^Mhdaaey12/Gje1^Mhdaaey12 involves: C3HeB/FeJ	abnormal lens development	J:136139
	abnormal lens fiber morphology	J:136139
	abnormal lens morphology	J:136139
	abnormal lens vesicle development	J:136139
	abnormal retina morphology	J:136139
	microphthalmia	J:136139
	retina fold	J:136139
	small lens	J:136139
Gje1^{tm1b(EUCOMM)Hmgu}/Gje1^{tm1b(EUCOMM)Hmgu} involves: 129S4/SvJaeSor * C57BL/6N	no abnormal phenotype detected	J:231436

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 04/16/2024 MGI 6.23