lipid storage disease Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A lysosomal storage disease that involves the accumulation of harmful amounts of lipids (fats) in some of the body's cells and tissues. (Human Disease Ontology, DOID_9455)
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Genes

8 genes associated with the disease lipid storage disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
SGPP1 sphingosine-1-phosphate phosphatase 1 2.39414
CERS4 ceramide synthase 4 1.64122
ATP10D ATPase, class V, type 10D 1.29434
SPTLC3 serine palmitoyltransferase, long chain base subunit 3 1.03105
FADS3 fatty acid desaturase 3 0.905535
CLN8 ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation) 0.256228
ADRB1 adrenoceptor beta 1 0.197766
NTRK3 neurotrophic tyrosine kinase, receptor, type 3 0.064973