lipidosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description abnormal fat metabolism with increased accumulation of specific lipids in tissue (Mammalian Phenotype Ontology, MP_0008570)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008570
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Genes

8 gene mutations causing the lipidosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCG1 ATP-binding cassette, sub-family G (WHITE), member 1
ACADL acyl-CoA dehydrogenase, long chain
APOC3 apolipoprotein C-III
CHD2 chromodomain helicase DNA binding protein 2
NPC1 Niemann-Pick disease, type C1
NPC2 Niemann-Pick disease, type C2
PEX7 peroxisomal biogenesis factor 7
PHYH phytanoyl-CoA 2-hydroxylase