TARBP2 TARBP2 subunit of RISC loading complex
Information
- Symbol
- TARBP2
- Type
- protein-coding
- Description
- TARBP2 subunit of RISC loading complex
- Entrez Gene ID
- 6895
- Genome
- hg19
- Position
- chr12:53,895,067-53,900,215
- Genome
- hg38
- Position
- chr12:53,501,283-53,506,431
- MIM
- 605053 OMIM
- HGNC
- HGNC:11569 HGNC
- Ensembl
- ENSG00000139546 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 4 |
| Uncertain significance | 0 | 30 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
34 |
 |
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
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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| 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 | LOQS |
| SYNONYM | TRBP |
| SYNONYM | TRBP1 |
| SYNONYM | TRBP2 |
| MIM | 605053 OMIM |
| HGNC | HGNC:11569 HGNC |
| Ensembl | ENSG00000139546 Ensembl |
| AllianceGenome | HGNC:11569 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000456234.6 | hg38 | chr12 | 53,500,953 | 53,506,424 | 5,472 |
| ENST00000552857.5 | hg38 | chr12 | 53,501,274 | 53,506,229 | 4,956 |
| ENST00000394357.6 | hg38 | chr12 | 53,501,619 | 53,506,412 | 4,794 |
| ENST00000710362.1 | hg38 | chr12 | 53,501,283 | 53,506,431 | 5,149 |
| ENST00000266987.7 | hg38 | chr12 | 53,501,283 | 53,506,431 | 5,149 |
| ENST00000456234.6 | hg19 | chr12 | 53,894,737 | 53,900,208 | 5,472 |
| ENST00000266987.7 | hg19 | chr12 | 53,895,067 | 53,900,215 | 5,149 |
| ENST00000394357.6 | hg19 | chr12 | 53,895,403 | 53,900,196 | 4,794 |
| ENST00000552857.5 | hg19 | chr12 | 53,895,058 | 53,900,013 | 4,956 |
| ENST00000710362.1 | hg19 | chr12 | 53,895,067 | 53,900,215 | 5,149 |
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