Entity Details

Primary name FCN3
Entity type gene
Source Source Link

Details

PrimaryID8547
RefseqGeneNG_016279
SymbolFCN3
Nameficolin 3
Chromosome1
Location1p36.11
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1999-12-14
ModificationDate2021-06-19

Ontological Relatives

UniProt IDsFCN3_HUMAN

GO terms

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GOName
GO:0001867 complement activation, lectin pathway
GO:0003823 antigen binding
GO:0005576 extracellular region
GO:0005581 collagen trimer
GO:0005615 extracellular space
GO:0006956 complement activation
GO:0030246 carbohydrate binding
GO:0043654 recognition of apoptotic cell
GO:0046597 negative regulation of viral entry into host cell
GO:0046872 metal ion binding
GO:0051607 defense response to virus
GO:0062023 collagen-containing extracellular matrix
GO:0072562 blood microparticle
GO:1902679 negative regulation of RNA biosynthetic process

Diseases

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Disease IDSourceNameDescription
613860 OMIMFicolin 3 deficiency (FCN3D)A disorder characterized by immunodeficiency, recurrent infections, brain abscesses and recurrent warts on the fingers. Affected individuals have normal levels of lymphocytes, normal T-cell responses, and normal antibodies, but a selective deficient antibody response to pneumococcal polysaccharide vaccine. The disease is caused by variants affecting the gene represented in this entry.

Interactions

8 interactions