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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Iglon5
IgLON family member 5
MGI:2686277
18 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Iglon5em1(IMPC)Mbp/Iglon5em1(IMPC)Mbp
C57BL/6NCrl-Iglon5em1(IMPC)Mbp/Mmucd
abnormal eye morphology J:211773
abnormal kidney morphology J:211773
abnormal liver morphology J:211773
abnormal lymph node morphology J:211773
abnormal nest building behavior J:345884
abnormal skin morphology J:211773
abnormal spleen morphology J:211773
abnormal sucrose solution preference J:345884
anhedonia J:345884
enlarged kidney J:211773
enlarged lymph nodes J:211773
enlarged seminal vesicle J:211773
enlarged spleen J:211773
hyperactivity J:345884
impaired balance J:345884
increased vertical activity J:345884
normal nervous system phenotype J:345884
small kidney J:211773

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
04/16/2024
MGI 6.23
The Jackson Laboratory