fm Phenotype Annotations

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

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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