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PTX3 (pentraxin 3)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
5806
Gene nameGene Name - the full gene name approved by the HGNC.
Pentraxin 3
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
PTX3
SynonymsGene synonyms aliases
TNFAIP5, TSG-14
ChromosomeChromosome number
3
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3q25.32
SummarySummary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the pentraxin protein family. The expression of this protein is induced by inflammatory cytokines in response to inflammatory stimuli in several mesenchymal and epithelial cell types, particularly endothelial cells and mononuclear phagocytes. The protein promotes fibrocyte differentiation and is involved in regulating inflammation and complement activation. It also plays a role in angiogenesis and tissue remodeling. The protein serves as a biomarker for several inflammatory conditions. [provided by RefSeq, Jun 2016]
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT005954 hsa-miR-21-5p Luciferase reporter assay 21131358
MIRT054880 hsa-miR-224-5p Luciferase reporter assay, qRT-PCR, Western blot 24470395
MIRT732871 hsa-miR-9-5p ELISA, qRT-PCR 28031262
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001550 Process Ovarian cumulus expansion IEA
GO:0001849 Function Complement component C1q complex binding IBA 21873635
GO:0001849 Function Complement component C1q complex binding IDA 23544079
GO:0001872 Function (1->3)-beta-D-glucan binding IEA
GO:0001878 Process Response to yeast IEA
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID P26022
Protein name Pentraxin-related protein PTX3 (Pentaxin-related protein PTX3) (Tumor necrosis factor alpha-induced protein 5) (TNF alpha-induced protein 5) (Tumor necrosis factor-inducible gene 14 protein) (TSG-14)
Protein function Plays a role in the regulation of innate resistance to pathogens, inflammatory reactions, possibly clearance of self-components and female fertility.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00354 Pentaxin
181 379
Pentaxin family
Domain
Sequence
MHLLAILFCALWSAVLAENSDDYDLMYVNLDNEIDNGLHPTEDPTPCACGQEHSEWDKLF
IMLENSQMRERMLLQATDDVLRGELQRLREELGRLAESLARPCAPGAPAEARLTSALDEL
LQATRDAGRRLARMEGAEAQRPEEAGRALAAVLEELRQTRADLHAVQGWAARSWLPAGCE
TAILFPMRSKKIFGSVHPVRPMRLESFSACIWVKATDVLNKTILFSYGTKRNPYEIQLYL
SYQSIVFVVGGEENKLVAEAMVSLGRWTHLCGTWNSEEGLTSLWVNGELAATTVEMATGH
IVPEGGILQIGQEKNGCCVGGGFDETLAFSGRLTGFNIWDSVLSNEEIRETGGAESCHIR
GNIVGWGVTEIQPHGGAQY
VS
Sequence length 381
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
Reactome
    Neutrophil degranulation
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Pulmonary fibrosis Pulmonary Fibrosis rs121918666, rs199422300, rs121917737, rs121917834, rs199422294, rs201159197, rs199422297, rs199422305, rs751381953, rs876661305, rs878853260, rs863223336, rs786205702, rs1555811762, rs1060502990, rs1555903332, rs1554038539, rs1554042899, rs938938578 22210019
Unknown
Disease name Disease term dbSNP ID References
Mental depression Unipolar Depression, Major Depressive Disorder rs587778876, rs587778877 14603263
Alveolitis Alveolitis, Fibrosing 22210019
Arsenic encephalopathy Arsenic Encephalopathy 16835338
Dermatologic disorders Dermatologic disorders 16835338

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