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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Gje1
gap junction protein, epsilon 1
MGI:1923993
13 phenotypes from 3 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Gje1em1(IMPC)H/Gje1em1(IMPC)H
C57BL/6NTac-Gje1em1(IMPC)H/H
decreased circulating serum albumin level J:211773
Gje1Mhdaaey12/Gje1+
C3HeB/FeJ-Gje1Mhdaaey12/Ieg
microphthalmia J:86685
Gje1Mhdaaey12/Gje1+
involves: C3HeB/FeJ
abnormal lens fiber morphology J:136139
cornea opacity J:136139
increased cornea thickness J:136139
microphthalmia J:136139
polar cataract J:136139
small lens J:136139
Gje1Mhdaaey12/Gje1Mhdaaey12
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
Gje1tm1b(EUCOMM)Hmgu/Gje1tm1b(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)
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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory