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

Gene information from NCBI Gene. Variant classifications from ClinVar.