Details

Home Details


Basic information of TREM2 :

Official Symbol of Gene TREM2
Species Homo sapiens
Entrez Gene ID 54209
Official Full Name triggering receptor expressed on myeloid cells 2
Also known as PLOSL2; TREM-2; Trem2a; Trem2b; Trem2c
Gene Type protein coding
dbXrefs Ensembl:ENSG00000095970 MIM:605086; AllianceGenome:HGNC:17761
Map Location 6p21.1
Variation Type SNP
refSNP ID rs75932628

Sample information of multiple sclerosis:

Detected Sample Peripheral blood
Sample Detail N/A
Detected Method PCR
Disease MS
Disease subtype N/A
Population N/A
Sample Size 1246 MS cases and 398 controls

Literature information of multiple sclerosis :

Pubmed ID 31362167
Year 2019
Title TREM2 R47H (rs75932628) variant is unlikely to contribute to Multiple Sclerosis susceptibility and severity in a large Greek MS cohort

Results of multiple sclerosis :

Risk Type Disease risk
Main Result This variant does not seem to play a determining role in the pathogenesis of MS, although further studies examining the presence of TREM2 mutations in other, phylogenetically different populations and the epigenetic regulation of this gene are needed in order to thoroughly investigate its role in MS.
Result Minor allele rs75932628-T frequency was reported between 0.0017 to 0.003 in European populations
Mechanism/Pathway TREM2 is a signaling protein which participates in the innate immune system by implication to inflammation, proliferation and phagocytosis.