complement C7

Summary
Gene Symbol
  • C7
Organism
Homo sapiens (human)
NCBI Gene
730
PubChem
730
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Complement alternate pathway
  • Direct protein sequencing
  • Disease variant
  • Disulfide bond
  • EGF-like domain
  • Glycoprotein
  • Membrane attack complex
  • Reference proteome
  • Repeat
  • Secreted
  • Signal
  • Sushi
Proteins
Displaying all 2 entries
UniProt Protein Name
Q05CI3
P10643
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
Potassium transporter
Functional Category
  • E: Amino acid transport and metabolism
  • P: Inorganic ion transport and metabolism
  • T: Signal transduction mechanisms
Displaying 1 entry
Gene Ontology
monoatomic ion transport
Disease
Disease Ontology
Displaying all 4 entries
DO ID Disease Name Source
DOID:0060300 complement component 7 deficiency
DOID:10976 membranous glomerulonephritis
DOID:11832 visual epilepsy
DOID:5844 myocardial infarction

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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