Gene: PCSK6

Alternate names for this Gene: PACE4|SPC4

Gene 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 initial autocatalytic processing event in the ER to generate a heterodimer which exits the ER and sorts to the trans-Golgi network where a second autocatalytic event takes place and the catalytic activity is acquired. The encoded protease is constitutively secreted into the extracellular matrix and expressed in many tissues, including neuroendocrine, liver, gut, and brain. This gene encodes one of the seven basic amino acid-specific members which cleave their substrates at single or paired basic residues. Some of its substrates include transforming growth factor beta related proteins, proalbumin, and von Willebrand factor. This gene is thought to play a role in tumor progression and left-right patterning. Alternatively spliced transcript variants encoding different isoforms have been identified.

Gene is located in Chromosome: 15

Location in Chromosome : 15q26.3

Description of this Gene: proprotein convertase subtilisin/kexin type 6

Type of Gene: protein-coding

Gene: PCSK6-AS1

Alternate names for this Gene:

Gene Summary:

Gene is located in Chromosome:

Location in Chromosome :

Description of this Gene:

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rs11855415 in PCSK6;PCSK6-AS1 gene and Dyslexia PMID 21051773 2011 PCSK6 is associated with handedness in individuals with dyslexia.

rs11855415 in PCSK6;PCSK6-AS1 gene and Functional Laterality PMID 21051773 2011 PCSK6 is associated with handedness in individuals with dyslexia.

rs11855415 in PCSK6;PCSK6-AS1 gene and Handedness PMID 21051773 2011 PCSK6 is associated with handedness in individuals with dyslexia.