multifocal hepatic necrosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description morphological changes resulting from multiple localized areas of pathological death of liver tissue; usually due to irreversible damage (Mammalian Phenotype Ontology, MP_0001655)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001655
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Genes

10 gene mutations causing the multifocal hepatic necrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGA aspartylglucosaminidase
CCR2 chemokine (C-C motif) receptor 2
CLCA2 chloride channel accessory 2
FOXP3 forkhead box P3
IKZF1 IKAROS family zinc finger 1 (Ikaros)
IL22 interleukin 22
SPTB spectrin, beta, erythrocytic
STAT1 signal transducer and activator of transcription 1, 91kDa
TGFB1 transforming growth factor, beta 1
UNC93B1 unc-93 homolog B1 (C. elegans)