Gene Information gene info

GENE:TREM2

GeneInfo:

GeneAttribute GeneDescription
GeneSymbol TREM2
FullNmae triggering receptor expressed on myeloid cells 2
LocusType gene with protein product
Status Approved
HGNC_id HGNC:17761
EnsembleID ENSG00000095970
Uniprot Q9NZC2

Protein Structure:

Gene Description in Publicaton:

GeneSymbol CellDeathType PMID Description GeneType
TREM2 autophagy 38538696 The 18 RCD signatures collected from previous studies. Supplementary Table of Figures.xlsx (https://github.com/zwxiangya/RCDscore) retulator signature
TREM2 autophagy 36341760 The PCD-related genes contained the key regulatory genes of twelve PCD patterns which is mentioned above. Genes were collected from GSEA gene sets, KEGG, review articles, and manual collation [10]. The ultimate gene list was the concatenation regulatory genes of twelve PCD patterns. regulator signature
TREM2 apoptosis 38538696 The 18 RCD signatures collected from previous studies. Supplementary Table of Figures.xlsx (https://github.com/zwxiangya/RCDscore) retulator signature

Go Annotation:

GeneSymbol Go id
TREM2 GO:0001530,GO:0001540,GO:0001774,GO:0001786,GO:0001934,GO:0002282,GO:0002588,GO:0002862,GO:0002931,GO:0004888,GO:0004888,GO:0005515,GO:0005543,GO:0005576,GO:0005886,GO:0005886,GO:0005886,GO:0005886,GO:0006910,GO:0006911,GO:0006959,GO:0007613,GO:0007613,GO:0008035,GO:0008289,GO:0008429,GO:0009986,GO:0010468,GO:0010507,GO:0010628,GO:0010628,GO:0010822,GO:0010875,GO:0010887,GO:0010891,GO:0010983,GO:0016020,GO:0019209,GO:0019216,GO:0030169,GO:0030316,GO:0032006,GO:0032008,GO:0032497,GO:0032499,GO:0032675,GO:0032691,GO:0032720,GO:0032733,GO:0033674,GO:0034136,GO:0034144,GO:0034151,GO:0034185,GO:0034186,GO:0034189,GO:0034241,GO:0034351,GO:0035176,GO:0038023,GO:0038023,GO:0038160,GO:0042834,GO:0043124,GO:0043277,GO:0044853,GO:0044877,GO:0045088,GO:0045672,GO:0045728,GO:0045960,GO:0048143,GO:0048678,GO:0048678,GO:0050714,GO:0050730,GO:0050730,GO:0050731,GO:0050766,GO:0050766,GO:0050829,GO:0050850,GO:0050850,GO:0050866,GO:0050921,GO:0051897,GO:0051898,GO:0055088,GO:0060075,GO:0060100,GO:0060100,GO:0060100,GO:0061518,GO:0061889,GO:0070269,GO:0070345,GO:0070374,GO:0070374,GO:0070374,GO:0070392,GO:0070891,GO:0071223,GO:0071224,GO:0071333,GO:0071396,GO:0071456,GO:0071640,GO:0071813,GO:0097028,GO:0097062,GO:0097110,GO:0098657,GO:0110089,GO:0120035,GO:0120035,GO:0120035,GO:0120146,GO:0140052,GO:0150062,GO:0150079,GO:0150079,GO:0150094,GO:0150094,GO:1900015,GO:1900016,GO:1900223,GO:1900223,GO:1900226,GO:1900226,GO:1901076,GO:1901224,GO:1901800,GO:1901980,GO:1902227,GO:1902531,GO:1903078,GO:1903082,GO:1903376,GO:1903753,GO:1903980,GO:1903980,GO:1903980,GO:1904093,GO:1904141,GO:1904141,GO:1904646,GO:1904951,GO:1905291,GO:1905581,GO:1905805,GO:1905808,GO:1905907,GO:1990782,GO:2000350,GO:2001171

KEGG Annotation:

GeneSymbol GeneID Pathway Pathway Name
TREM2 hsa:54209 path:hsa04380 Osteoclast differentiation - Homo sapiens (human)

Protein-Protein Interaction(String):

Signalink 3.0 modificators

Source Target Pmid Interactiontype Methods Database
TYROBP TREM2 11602640 23180781 physical association anti tag coimmunoprecipitation InnateDB

Source Target Pmid Interactiontype Methods Database
CEBPA TREM2 18971253 trascriptional regulation,stimulation inferred by curator TFlink
TRIM28 TREM2 18971253 trascriptional regulation,stimulation inferred by curator TFlink

Source Target Pmid Interactiontype Methods Database
URS00000EED18 TREM2 25416803 26949937 mrna cleavage,inhibition array technology,western blot,quantitative reverse transcription pcr,miRNA interference luciferase reporter assay TarBase

Source Target Pmid Interactiontype Methods Database
TYROBP TREM2 11602640 12080485 14525934 24234451 25348397 27898060 physical association anti bait coimmunoprecipitation,experimental interaction detection,in vivo ComPPI,HPRD,IntAct,OmniPath
PSEN1 TREM2 24234451 29611543 colocalization,association,physical association anti bait coimmunoprecipitation,anti tag coimmunoprecipitation,pull down,confocal microscopy IntAct
SEMA6D TREM2 16715077 27898060 N/A N/A OmniPath

Visualization