CD14

Gene Information
 
Gene Symbol
CD14
 
Aliases
-
 
Entrez Gene ID
929
 
Gene Name
CD14 molecule
 
Chromosomal Location
5q31.3
 
HGNC ID
 
Summary
The protein encoded by this gene is a surface antigen that is preferentially expressed on monocytes/macrophages. It cooperates with other proteins to mediate the innate immune response to bacterial lipopolysaccharide. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Mar 2010]
 
RefSeq DNA
 
RefSeq mRNA
  e!Ensembl
Gene
Transcript  
Protein

Gene Ontology (GO)

GO ID Ontology Function Evidence Reference
GO:0006909 Biological process Phagocytosis TAS 9548256
GO:0006915 Biological process Apoptotic process TAS 9548256
GO:0006954 Biological process Inflammatory response IBA 21873635
GO:0007166 Biological process Cell surface receptor signaling pathway TAS 8798531
GO:0031663 Biological process Lipopolysaccharide-mediated signaling pathway IBA 21873635
Protein Information
 
Protein Name
Monocyte differentiation antigen CD14, myeloid cell-specific leucine-rich glycoprotein
 
Function
Coreceptor for bacterial lipopolysaccharide (PubMed:1698311, PubMed:23264655). In concert with LBP, binds to monomeric lipopolysaccharide and delivers it to the LY96/TLR4 complex, thereby mediating the innate immune response to bacterial lipopolysaccharide (LPS) (PubMed:20133493, PubMed:23264655). Acts via MyD88, TIRAP and TRAF6, leading to NF-kappa-B activation, cytokine secretion and the inflammatory response (PubMed:8612135). Acts as a coreceptor for TLR2:TLR6 heterodimer in response to diacylated lipopeptides and for TLR2:TLR1 heterodimer in response to triacylated lipopeptides, these clusters trigger signaling from the cell surface and subsequently are targeted to the Golgi in a lipid-raft dependent pathway (PubMed:16880211). Binds electronegative LDL (LDL(-)) and mediates the cytokine release induced by LDL(-)
 
Refseq Proteins
 
UniProt
 
PDB
Pathways
 
KEGG
 
Reactome
 

MAPK signaling pathway
NF-kappa B signaling pathway
Phagosome
Toll-like receptor signaling pathway
Hematopoietic cell lineage
Pathogenic Escherichia coli infection
Salmonella infection
Pertussis
Legionellosis
Amoebiasis
Tuberculosis
Transcriptional misregulation in cancer
Acute myeloid leukemia

 

ER-Phagosome pathway
Caspase activation via Death Receptors in the presence of ligand
Toll Like Receptor 4 (TLR4) Cascade
Transfer of LPS from LBP carrier to CD14
MyD88:MAL(TIRAP) cascade initiated on plasma membrane
MyD88-independent TLR4 cascade
Toll Like Receptor TLR1:TLR2 Cascade
Toll Like Receptor TLR6:TLR2 Cascade
TRIF-mediated programmed cell death
MyD88 deficiency (TLR2/4)
IRAK4 deficiency (TLR2/4)
Regulation of TLR by endogenous ligand
Neutrophil degranulation
Activation of IRF3/IRF7 mediated by TBK1/IKK epsilon
IKK complex recruitment mediated by RIP1
TRAF6-mediated induction of TAK1 complex within TLR4 complex
IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation

Interactions
 
STRING MINT IntAct
ENSP00000304236 P08571 P08571
    View interactions
     

Associated Diseases

Disease groupDisease NameReferences
Blood Disorders
Anemia
Blood Coagulation Disorders
Kawasaki disease
Thrombocytopenia
Cardiovascular Diseases
Cardiovascular Abnormalities
References
 
 
PubMed ID Associated gene/s Associated condition Genetic Mutation Diagnostic Criteria Association with PCOS Ethnicity Conclusion
 
PCOS, Inflammation 
 
Rotterdam Criteria 
Direct 
38 PCOS patients and 40 controls (7 PCOS patients and 3 controls were downloaded from GEO dataset 34526) 
In conclusion, our data collectively provide a comprehensive bioinformatics analysis of DEGs in PCOS. Our results confirm that the inflammation and immune play important roles in the occurrence and development of PCOS. Meanwhile, TLR signaling pathway mediating inflammation and immune might be involved in the pathogenesis of PCOS, and TLR2, TLR8, CD14 may be core target genes. 

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