SCUBA

ELOVL5 — ELOVL fatty acid elongase 5

ELOVL5 belongs to a gene co-expression module in 3 of 28 SCUBA cell types. Each module groups genes that rise and fall together in that cell type; the genes it shares a module with are its closest co-expression partners there.

ELOVL5's module in each cell type

Cell typeModuleShares the module with
CD4⁺ T cellsNF-kB regulation
TCR/AP1/NFKb pathway
ARIH2, CD58, CYLD, DAD1, DERL1, EED, NFAT5, OTULIN +9 moreView in SCUBA
EndothelialER Calcium Stress
Stress
ACOT7, ATP2A2, CALU, GTF2A2, LYAR, PSMD7, RCC2, UFD1 +1 moreView in SCUBA
Innate lymphoid cellsIFN-driven ILC1 Activation
Inflammation
AFF3, AGPAT5, AKIRIN2, APMAP, ARF6, ARHGEF1, DNAJC1, DYNLT3 +21 moreView in SCUBA

About the gene

SynonymsdJ483K16.1, HELO1, SCA38
Chromosome6: 53267398-53349179
Predicted locationIntracellular, Membrane
Essential geneNo
Protein classDisease related genes, Enzymes, Human disease related genes, Metabolic proteins, Potential drug targets, Predicted intracellular proteins, Predicted membrane proteins
Molecular functionTransferase
Biological processFatty acid biosynthesis, Fatty acid metabolism, Lipid biosynthesis, Lipid metabolism

Function

Catalyzes the first and rate-limiting reaction of the four reactions that constitute the long-chain fatty acids elongation cycle. This endoplasmic reticulum-bound enzymatic process allows the addition of 2 carbons to the chain of long- and very long-chain fatty acids (VLCFAs) per cycle. Condensing enzyme that acts specifically toward polyunsaturated acyl-CoA with the higher activity toward C18:3(n-6) acyl-CoA. May participate in the production of monounsaturated and of polyunsaturated VLCFAs of different chain lengths that are involved in multiple biological processes as precursors of membrane lipids and lipid mediators (By similarity). In conditions where the essential linoleic and alpha linoleic fatty acids are lacking it is also involved in the synthesis of Mead acid from oleic acid (By similarity).

Human Protein Atlas · Open Targets · UniProt

Gene annotation from the Human Protein Atlas and UniProt; see sources & licences.