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PCSK9 gene

proprotein convertase subtilisin/kexin type 9

Key facts

Official symbol
PCSK9
Full name
PCSK9
Chromosome
1
Map location
1p32.3
Organism
Homo sapiens
NCBI Gene ID
255738
Also known as
FH3, FHCL3, HCHOLA3, LDLCQ1, NARC-1, NARC1

Function 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].

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Data source: NCBI Gene · alsesAI Gene Library