STAG3L5P-PVRIG2P-PILRB STAG3L5P-PVRIG2P-PILRB readthrough
Information
- Symbol
- STAG3L5P-PVRIG2P-PILRB
- Type
- ncRNA
- Description
- STAG3L5P-PVRIG2P-PILRB readthrough
- Entrez Gene ID
- 101752399
- Genome
- hg19
- Position
- chr7:99,933,737-99,965,454
- Genome
- hg38
- Position
- chr7:100,336,114-100,367,831
- HGNC
- HGNC:48898 HGNC
- Ensembl
- ENSG00000272752 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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0 |
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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 |
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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| 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 | FDFACT |
| SYNONYM | LOC101735302-LOC101752334-PILRB |
| SYNONYM | PILRB |
| HGNC | HGNC:48898 HGNC |
| Ensembl | ENSG00000272752 Ensembl |
| AllianceGenome | HGNC:48898 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000472646.1 | hg38 | chr7 | 100,351,256 | 100,358,292 | 7,037 |
| ENST00000483329.6 | hg38 | chr7 | 100,336,123 | 100,352,211 | 16,089 |
| ENST00000470714.5 | hg38 | chr7 | 100,336,104 | 100,352,489 | 16,386 |
| ENST00000310771.8 | hg38 | chr7 | 100,336,114 | 100,367,831 | 31,718 |
| ENST00000470714.5 | hg19 | chr7 | 99,933,727 | 99,950,112 | 16,386 |
| ENST00000310771.8 | hg19 | chr7 | 99,933,737 | 99,965,454 | 31,718 |
| ENST00000483329.6 | hg19 | chr7 | 99,933,746 | 99,949,834 | 16,089 |
| ENST00000472646.1 | hg19 | chr7 | 99,948,879 | 99,955,915 | 7,037 |
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