TREM2 triggering receptor expressed on myeloid cells 2

Information
Symbol
TREM2
Type
protein-coding
Description
triggering receptor expressed on myeloid cells 2
Entrez Gene ID
54209
Genome
hg19
Position
chr6:41,126,246-41,130,854
Genome
hg38
Position
chr6:41,158,508-41,163,116
MIM
605086 OMIM
HGNC
HGNC:17761 HGNC
Ensembl
ENSG00000095970 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 5 26
Likely pathogenic 0 18
Benign 7 20
Likely benign 0 114
Conflicting classifications of pathogenicity 0 20
Uncertain significance 0 144
Ranking
ClinVar
0
0
56
240
6
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
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Variant name Gene AA change CDS Japanese
frequency
TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence
Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM PLOSL2
SYNONYM TREM-2
SYNONYM Trem2a
SYNONYM Trem2b
SYNONYM Trem2c
MIM 605086 OMIM
HGNC HGNC:17761 HGNC
Ensembl ENSG00000095970 Ensembl
AllianceGenome HGNC:17761
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000373113.8 hg38 chr6 41,158,508 41,163,116 4,609
ENST00000373122.8 hg38 chr6 41,158,506 41,163,103 4,598
ENST00000338469.3 hg38 chr6 41,158,507 41,163,186 4,680
ENST00000373122.8 hg19 chr6 41,126,244 41,130,841 4,598
ENST00000338469.3 hg19 chr6 41,126,245 41,130,924 4,680
ENST00000373113.8 hg19 chr6 41,126,246 41,130,854 4,609
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