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Allele : fm foam cell reticulosis
Primary Identifier  MGI:1856873 Allele Type  Spontaneous
Gene  fm Inheritance Mode  Recessive
Strain of Origin  CBA/H Is Recombinase  false
Is Wild Type  false
description  The disease resembles a group of lipid storage diseases in human and is most similar to Niemann-Pick disease, type C (J:5696).
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

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6 Publication categories

Trail: Allele




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