TLR2 toll like receptor 2
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 24 |
| Likely benign | 0 | 28 |
| Conflicting classifications of pathogenicity | 0 | 2 |
| not provided | 1 | 4 |
| risk factor | 0 | 4 |
| Uncertain significance | 0 | 72 |
Ranking
| ClinVar | |
|---|---|
![]() |
0 |
![]() |
0 |
![]() |
6 |
![]() |
110 |
![]() |
8 |
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 | : |
|
| Search word | : | |
| Filtering | : |
| 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 | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | CD282 |
| SYNONYM | TIL4 |
| MIM | 603028 OMIM |
| HGNC | HGNC:11848 HGNC |
| Ensembl | ENSG00000137462 Ensembl |
| AllianceGenome | HGNC:11848 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000642580.1 | hg38 | chr4 | 153,684,265 | 153,705,702 | 21,438 |
| ENST00000646900.2 | hg38 | chr4 | 153,684,070 | 153,705,696 | 21,627 |
| ENST00000260010.7 | hg38 | chr4 | 153,684,244 | 153,705,699 | 21,456 |
| ENST00000642700.2 | hg38 | chr4 | 153,684,280 | 153,706,260 | 21,981 |
| ENST00000643501.2 | hg38 | chr4 | 153,684,280 | 153,706,260 | 21,981 |
| ENST00000646219.2 | hg38 | chr4 | 153,684,261 | 153,706,260 | 22,000 |
| ENST00000714435.1 | hg38 | chr4 | 153,684,276 | 153,705,326 | 21,051 |
| ENST00000714436.1 | hg38 | chr4 | 153,684,280 | 153,705,452 | 21,173 |
| ENST00000714433.1 | hg38 | chr4 | 153,684,079 | 153,705,699 | 21,621 |
| ENST00000714434.1 | hg38 | chr4 | 153,684,253 | 153,705,702 | 21,450 |
| ENST00000714431.1 | hg38 | chr4 | 153,684,050 | 153,705,697 | 21,648 |
| ENST00000714432.1 | hg38 | chr4 | 153,684,070 | 153,705,696 | 21,627 |
| ENST00000714431.1 | hg19 | chr4 | 154,605,202 | 154,626,849 | 21,648 |
| ENST00000714432.1 | hg19 | chr4 | 154,605,222 | 154,626,848 | 21,627 |
| ENST00000646900.2 | hg19 | chr4 | 154,605,222 | 154,626,848 | 21,627 |
| ENST00000714433.1 | hg19 | chr4 | 154,605,231 | 154,626,851 | 21,621 |
| ENST00000260010.7 | hg19 | chr4 | 154,605,396 | 154,626,851 | 21,456 |
| ENST00000714434.1 | hg19 | chr4 | 154,605,405 | 154,626,854 | 21,450 |
| ENST00000646219.2 | hg19 | chr4 | 154,605,413 | 154,627,412 | 22,000 |
| ENST00000642580.1 | hg19 | chr4 | 154,605,417 | 154,626,854 | 21,438 |
| ENST00000714435.1 | hg19 | chr4 | 154,605,428 | 154,626,478 | 21,051 |
| ENST00000714436.1 | hg19 | chr4 | 154,605,432 | 154,626,604 | 21,173 |
| ENST00000642700.2 | hg19 | chr4 | 154,605,432 | 154,627,412 | 21,981 |
| ENST00000643501.2 | hg19 | chr4 | 154,605,432 | 154,627,412 | 21,981 |
Genome browser




