rs55747707
This is a regulatory region variant variant in the MLXIPL gene.
▶GWAS Catalog Trait Associations (68)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (68)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
triglyceride measurement
triglycerides to total lipids in very large HDL percentage
triglycerides to total lipids in large HDL percentage
phospholipids in very large HDL measurement
total lipids in very large HDL measurement
cholesteryl esters in large HDL measurement
cholesterol in large HDL measurement
phospholipids:total lipids ratio
free cholesterol in large HDL measurement
HDL particle size
About MLXIPL
This gene encodes a basic helix-loop-helix leucine zipper transcription factor of the Myc/Max/Mad superfamily. This protein forms a heterodimeric complex and binds and activates, in a glucose-dependent manner, carbohydrate response element (ChoRE) motifs in the promoters of triglyceride synthesis genes. The gene is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]
View all MLXIPL variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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