TREM1 triggering receptor expressed on myeloid cells 1
Information
- Symbol
- TREM1
- Type
- protein-coding
- Description
- triggering receptor expressed on myeloid cells 1
- Entrez Gene ID
- 54210
- Genome
- hg19
- Position
- chr6:41,241,343-41,254,420
- Genome
- hg38
- Position
- chr6:41,273,605-41,286,682
- MIM
- 605085 OMIM
- HGNC
- HGNC:17760 HGNC
- Ensembl
- ENSG00000124731 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 6 |
| Likely benign | 0 | 8 |
| Uncertain significance | 0 | 32 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
46 |
 |
0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
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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
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| 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
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| Category | : |
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| 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 | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | CD354 |
| SYNONYM | TREM-1 |
| MIM | 605085 OMIM |
| HGNC | HGNC:17760 HGNC |
| Ensembl | ENSG00000124731 Ensembl |
| AllianceGenome | HGNC:17760 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000589614.5 | hg38 | chr6 | 41,267,926 | 41,286,665 | 18,740 |
| ENST00000591620.1 | hg38 | chr6 | 41,279,539 | 41,286,682 | 7,144 |
| ENST00000244709.9 | hg38 | chr6 | 41,273,605 | 41,286,682 | 13,078 |
| ENST00000334475.10 | hg38 | chr6 | 41,275,621 | 41,286,682 | 11,062 |
| ENST00000589614.5 | hg19 | chr6 | 41,235,664 | 41,254,403 | 18,740 |
| ENST00000244709.9 | hg19 | chr6 | 41,241,343 | 41,254,420 | 13,078 |
| ENST00000334475.10 | hg19 | chr6 | 41,243,359 | 41,254,420 | 11,062 |
| ENST00000591620.1 | hg19 | chr6 | 41,247,277 | 41,254,420 | 7,144 |
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