Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10875
Gene name Gene Name - the full gene name approved by the HGNC.
Fibrinogen like 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
FGL2
Synonyms (NCBI Gene) Gene synonyms aliases
T49, pT49
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7q11.23
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a secreted protein that is similar to the beta- and gamma-chains of fibrinogen. The carboxyl-terminus of the encoded protein consists of the fibrinogen-related domains (FRED). The encoded protein forms a tetrameric comp
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT018781 hsa-miR-335-5p Microarray 18185580
MIRT030088 hsa-miR-26b-5p Microarray 19088304
MIRT440643 hsa-miR-155-5p HITS-CLIP 22473208
MIRT440643 hsa-miR-155-5p HITS-CLIP 22473208
MIRT996284 hsa-miR-1267 CLIP-seq
Transcription factors
Transcription factor Regulation Reference
SP1 Unknown 11170750
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0002291 Process T cell activation via T cell receptor contact with antigen bound to MHC molecule on antigen presenting cell IEA
GO:0002605 Process Negative regulation of dendritic cell antigen processing and presentation IEA
GO:0002617 Process Negative regulation of macrophage antigen processing and presentation IEA
GO:0005102 Function Signaling receptor binding IBA 21873635
GO:0005201 Function Extracellular matrix structural constituent RCA 28327460
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605351 3696 ENSG00000127951
Protein
UniProt ID Q14314
Protein name Fibroleukin (Fibrinogen-like protein 2) (pT49)
Protein function May play a role in physiologic lymphocyte functions at mucosal sites.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00147 Fibrinogen_C 209 435 Fibrinogen beta and gamma chains, C-terminal globular domain Domain
Tissue specificity TISSUE SPECIFICITY: Constitutively expressed in cytotoxic T-cells.
Sequence
MKLANWYWLSSAVLATYGFLVVANNETEEIKDERAKDVCPVRLESRGKCEEAGECPYQVS
LPPLTIQLPKQFSRIEEVFKEVQNLKEIVNSLKKSCQDCKLQADDNGDPGRNGLLLPSTG
APGEVGDNRVRELESEVNKLSSELKNAKEEINVLHGRLEKLNLVNMNNIENYVDSKVANL
TFVVNSLDGKCSKCPSQEQIQSRPVQHLIYKDCSDYYAIGKRSSETYRVTPDPKNSSFEV
YCDMETMGGGWTVLQARLDGSTNFTRTWQDYKAGFGNLRREFWLGNDKIHLLTKSKEMIL
RIDLEDFNGVELYALYDQFYVANEFLKYRLHVGNYNGTAGDALRFNKHYNHDLKFFTTPD
KDNDRYPSGNCGLYYSSGWWFDACLSANLNGKYYHQKYRGVRNGIFWGTWPGVSEAHPGG
YKSSFKEAKMMIRPK
HFKP
Sequence length 439
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Neutrophil degranulation
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Dermatitis Dermatitis, Allergic Contact rs61816761, rs150597413, rs138726443, rs201356558, rs149484917, rs372754256, rs747301529, rs567795279, rs745915174 17374397
Associations from Text Mining
Disease Name Relationship Type References
Acute Disease Associate 36755239
Acute On Chronic Liver Failure Associate 23067542
Aortic Dissection Associate 36755239
Breast Neoplasms Inhibit 32716910
Carcinoma Hepatocellular Associate 18715028
Carcinoma Non Small Cell Lung Associate 36969247
Carcinoma Renal Cell Stimulate 28978925
Colitis Ulcerative Stimulate 24287641
Colorectal Neoplasms Associate 25129313, 38036953
Communicable Diseases Associate 38310908