TREML1 triggering receptor expressed on myeloid cells like 1
Information
- Symbol
- TREML1
- Type
- protein-coding
- Description
- triggering receptor expressed on myeloid cells like 1
- Entrez Gene ID
- 340205
- Genome
- hg19
- Position
- chr6:41,117,075-41,122,085
- Genome
- hg38
- Position
- chr6:41,149,337-41,154,347
- MIM
- 609714 OMIM
- HGNC
- HGNC:20434 HGNC
- Ensembl
- ENSG00000161911 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 34 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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34 |
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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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
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Target data | : |
MGeND data only
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | GLTL1825 |
SYNONYM | PRO3438 |
SYNONYM | TLT-1 |
SYNONYM | TLT1 |
SYNONYM | dJ238O23.3 |
MIM | 609714 OMIM |
HGNC | HGNC:20434 HGNC |
Ensembl | ENSG00000161911 Ensembl |
AllianceGenome | HGNC:20434 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000373127.8 | hg38 | chr6 | 41,149,342 | 41,154,337 | 4,996 |
ENST00000426005.7 | hg38 | chr6 | 41,149,337 | 41,154,347 | 5,011 |
ENST00000437044.2 | hg38 | chr6 | 41,149,604 | 41,154,332 | 4,729 |
ENST00000426005.7 | hg19 | chr6 | 41,117,075 | 41,122,085 | 5,011 |
ENST00000373127.8 | hg19 | chr6 | 41,117,080 | 41,122,075 | 4,996 |
ENST00000437044.2 | hg19 | chr6 | 41,117,342 | 41,122,070 | 4,729 |
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