C-type lectin domain family 7 member A

Summary
UniProt ID
Q9BXN2
Gene Symbol
  • CLEC7A
  • BGR
  • CLECSF12
  • DECTIN1
Organism
Homo sapiens (human)
External Links
GlyGen
Q9BXN2
PubChem
Q9BXN2
The Human Metabolome Database
HMDBP12648
The O-GlcNAc Database
Q9BXN2
Annotation
Keyword
  • Alternative splicing
  • Cell membrane
  • Cytoplasm
  • Disulfide bond
  • Glycoprotein
  • Inflammatory response
  • Innate immunity
  • Lectin
  • Metal-binding
  • Phosphoprotein
  • Receptor
  • Reference proteome
  • Signal-anchor
  • Transmembrane helix
Gene Ontology (GO)
Sequence
MEYHPDLENLDEDGYTQLHFDSQSNTRIAVVSEKGSCAASPPWRLIAVILGILCLVILVIAVVLGTMAIWRSNSGSNTLENGYFLSRNKENHSQPTQSSLEDSVTPTKAVKTTGVLSSPCPPNWIIYEKSCYLFSMSLNSWDGSKRQCWQLGSNLLKIDSSNELGFIVKQVSSQPDNSFWIGLSRPQTEVPWLWEDGSTFSSNLFQIRTTATQENPSPNCVWIHVSVIYDQLCSVPSYSICEKKFSM
Glycosylation Sites
Displaying all 3 entries
Position Description PubMed ID GlyTouCan ID Source
91 N-linked (GlcNAc...) asparagine
112
153
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying 1 entry
Pathway Name Organism
CLEC7A (Dectin-1) signaling Homo sapiens
Disease
Displaying entries 1 - 10 of 120 in total
DO ID Disease Name Source
DOID:869 cholesteatoma
DOID:0040085 bacterial sepsis
DOID:12663 blastomycosis
DOID:0050133 superficial mycosis
DOID:0050167 autoimmune polyendocrine syndrome type 1
DOID:0050486 exanthem
DOID:0050589 inflammatory bowel disease
DOID:0050734 congenital intrinsic factor deficiency
DOID:0060041 autism spectrum disorder
DOID:0060180 colitis

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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: August 19, 2024