PCSK7

proprotein convertase subtilisin/kexin type 7

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. It encodes a type 1 membrane bound protease that is expressed in many tissues, including neuroendocrine, liver, gut, and brain. The encoded protein undergoes an initial autocatalytic processing event in the ER and then sorts to the trans-Golgi network through endosomes where a second autocatalytic event takes place and the catalytic activity is acquired. This gene encodes one of the seven basic amino acid-specific members which cleave their substrates at single or paired basic residues. It can process proalbumin and is thought to be responsible for the activation of HIV envelope glycoproteins gp160 and gp140. This gene has been implicated in the transcriptional regulation of housekeeping genes and plays a role in the regulation of iron metabolism. A t(11;14)(q23;q32) chromosome translocation associated with B-cell lymphoma occurs between this gene and its inverted counterpart. [provided by RefSeq, Feb 2014]

Known Variants53 total

rsidPosition (GRCh37)AllelesClassClinVar
rs20159830111:117,076,741G/A—benign
rs76264433611:117,076,783T/G—uncertain significance
rs76606034411:117,076,787G/C—uncertain significance
rs36960691711:117,076,874C/T—uncertain significance
rs123721274011:117,077,011T/C—uncertain significance
rs254278495811:117,077,018C/T—uncertain significance
rs52901158711:117,077,065A/G—uncertain significance
rs56683310511:117,077,478G/A—likely benign
rs74778888911:117,077,810C/G—uncertain significance
rs20208706611:117,078,679G/A—benign
rs59631411:117,078,702A/C—likely benign
rs178461711:117,079,433A/G——
rs55576671311:117,079,547C/T——
rs20203827511:117,079,626G/C—uncertain significance
rs77198613111:117,079,670T/G—uncertain significance
rs76852045311:117,079,688C/T—uncertain significance
rs75540105111:117,079,723A/G—likely benign
rs17105211:117,081,763C/T——
rs11176545911:117,083,373T/A——
rs6190648711:117,088,821C/Tintron variant—
rs76424381511:117,089,206G/A—uncertain significance
rs37527778711:117,089,251C/T—uncertain significance
rs203207732011:117,089,254A/G—uncertain significance
rs37391630811:117,089,867C/T—likely benign
rs253973991611:117,089,879T/C—uncertain significance
rs92900100111:117,090,318T/C—uncertain significance
rs23691811:117,091,609G/A——
rs7862878311:117,092,051C/Tregulatory region variant—
rs128217420111:117,093,929T/C—uncertain significance
rs95397678511:117,093,931C/T—uncertain significance
rs37287833911:117,094,803C/T—uncertain significance
rs54637652211:117,095,153C/A——
rs253975410811:117,095,464G/C—uncertain significance
rs77968512311:117,095,466C/T—uncertain significance
rs120400397711:117,097,963G/A—uncertain significance
rs253976073411:117,098,007T/C—uncertain significance
rs14320902411:117,098,029C/T—uncertain significance
rs203250618711:117,098,982C/T—uncertain significance
rs75847496011:117,099,060G/A—likely benign
rs11180921211:117,099,537T/A——
rs493836111:117,099,941G/T——
rs20105114711:117,100,109G/A—uncertain significance
rs159180812911:117,100,114C/T—likely benign
rs20059714711:117,100,178C/T—uncertain significance
rs75813931411:117,100,221G/C—uncertain significance
rs14542237711:117,100,298C/T—uncertain significance
rs20178143411:117,100,340G/A—uncertain significance
rs203256615711:117,100,362C/T—uncertain significance
rs37598157811:117,100,371C/T—uncertain significance
rs159180856111:117,100,374C/T—uncertain significance
rs203256939511:117,100,416T/G—likely benign
rs76738836311:117,100,437C/T—uncertain significance
rs118558509411:117,100,532T/C—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.