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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
fm
foam cell reticulosis
MGI:95563
22 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
fm/fm
involves: CBA/H
abnormal cerebellar cortex morphology J:5417
abnormal cerebellum morphology J:5417
abnormal cerebral hemisphere morphology J:5417
abnormal cholesterol level J:5112
abnormal endoplasmic reticulum morphology J:5417
abnormal liver morphology J:275, J:5417
abnormal lymph node morphology J:275
abnormal neuron morphology J:275
abnormal Peyer's patch morphology J:275
abnormal Purkinje cell morphology J:5417
abnormal sphingomyelin level J:5112
abnormal spleen morphology J:275, J:5417
abnormal thymus morphology J:275
cachexia J:5696
decreased body weight J:275
decreased locomotor activity J:275
foam cell reticulosis J:275
normal nervous system phenotype J:5696
neuronal cytoplasmic inclusions J:5417
premature death J:275, J:5696
sphingomyelinosis J:5112
weight loss J:275

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
04/23/2024
MGI 6.23
The Jackson Laboratory