proprotein convertase subtilisin/kexin type 1

Summary
Gene Symbol
  • PCSK1
Organism
Homo sapiens (human)
NCBI Gene
5122
PubChem
5122
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Calcium
  • Cleavage on pair of basic residues
  • Cytoplasmic vesicle
  • Disease variant
  • Disulfide bond
  • Glycoprotein
  • Obesity
  • Reference proteome
  • Serine protease
  • Signal
  • Zymogen
Proteins
Displaying 1 entry
UniProt Protein Name
P29120
  • Prohormone convertase 1
  • Proprotein convertase 1
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
FURIN
Functional Category
  • E: Amino acid transport and metabolism
  • Q: Secondary metabolites biosynthesis, transport and catabolism
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying all 9 entries
DO ID Disease Name Source
DOID:0111698 proprotein convertase 1/3 deficiency
DOID:11832 visual epilepsy
DOID:1459 hypothyroidism
DOID:1799 islet cell tumor
DOID:28 endocrine system disease
DOID:4195 hyperglycemia
DOID:7998 hyperthyroidism
DOID:9352 type 2 diabetes mellitus
DOID:9970 obesity

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International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024