Reference Gene

Gene name Alias Species Exons Type Paralogs EC number OMIM
PCSK9 proprotein convertase subtilisin/kexin type 9 FH3 , PC9 , FHCL3 , NARC1 , LDLCQ1 , NARC-1 , HCHOLA3 Homo sapiens 15 protein-coding TPP2 , MBTPS1 3.4.21.- 607786

Summary

This gene encodes a member of the subtilisin-like proprotein convertase family, which includes proteases that process protein and peptide precursors trafficking through regulated or constitutive branches of the secretory pathway. The encoded protein undergoes an autocatalytic processing event with its prosegment in the ER and is constitutively secreted as an inactive protease into the extracellular matrix and trans-Golgi network. It is expressed in liver, intestine and kidney tissues and escorts specific receptors for lysosomal degradation. It plays a role in cholesterol and fatty acid metabolism. Mutations in this gene have been associated with autosomal dominant familial hypercholesterolemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]

GeneOntology

Gene Loss events - PCSK9 (185 results)

GL_ID Species Order Gene Loss Mechanism Loss Type Lineage Specific Citation
GL_VA33G4 Bos javanicus Artiodactyla Exon(s) deletion Full Pecora 10.1007/s10709-021-00113-x
GL_VGOE2E Elaphurus davidianus Artiodactyla Exon(s) deletion Full 10.1007/s10709-021-00113-x
GL_VYK6US Mustela nigripes Carnivora Exon(s) deletion Full 10.1007/s10709-021-00113-x
GL_WCDVNW Felis margarita Carnivora Exon(s) deletion Full Felidae 10.1007/s10709-021-00113-x
GL_WNL97X Moschus moschiferus Artiodactyla Exon(s) deletion Full 10.1007/s10709-021-00113-x
GL_WRRXQI Pseudois nayaur Artiodactyla Exon(s) deletion Full Pecora 10.1007/s10709-021-00113-x
GL_WSWKQL Ursus maritimus Carnivora Exon(s) deletion Full Ursidae 10.1007/s10709-021-00113-x
GL_X3NVAA Ovis aries musimon Artiodactyla Exon(s) deletion Full Pecora 10.1007/s10709-021-00113-x
GL_XGS3IZ Ovis ammon Artiodactyla Exon(s) deletion Full Pecora 10.1007/s10709-021-00113-x
GL_XOLXSS Helogale parvula Carnivora Exon(s) deletion Full 10.1007/s10709-021-00113-x