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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Olfm2
olfactomedin 2
MGI:3045350
10 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Olfm2tm1.1Sit/Olfm2tm1.1Sit
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N
abnormal anxiety-related response J:217902
abnormal motor capabilities/coordination/movement J:217902
abnormal optic nerve morphology J:217902
abnormal visual evoked potential J:217902
decreased locomotor activity J:217902
decreased vertical activity J:217902
normal growth/size/body region phenotype J:217902
impaired coordination J:217902
normal mortality/aging J:217902
normal vision/eye phenotype J:217902

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