complement C9

Summary
Gene Symbol
  • C9
Organism
Homo sapiens (human)
NCBI Gene
735
PubChem
735
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Age-related macular degeneration
  • Complement alternate pathway
  • Direct protein sequencing
  • Disease variant
  • Disulfide bond
  • EGF-like domain
  • Glycoprotein
  • Membrane attack complex
  • Phosphoprotein
  • Reference proteome
  • Secreted
  • Signal
  • Target cell membrane
  • Transmembrane beta strand
Proteins
Displaying 1 entry
UniProt Protein Name
P02748
Gene Ontology (GO)
GO Hierarchy
Displaying 1 entry
GO Term Evidence Code PMID
protein binding
OrthoDB (Group)
Group level
Eukaryota
Group Name
uncharacterized protein
Functional Category
  • M: Cell wall/membrane/envelope biogenesis
  • O: Posttranslational modification, protein turnover, chaperones
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying all 5 entries
DO ID Disease Name Source
DOID:0060303 complement component 9 deficiency
DOID:0080322 polycystic kidney disease
DOID:0110027 age related macular degeneration 15
DOID:2559 opiate dependence
DOID:898 autosomal dominant polycystic kidney disease

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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