LINC02052 long intergenic non-protein coding RNA 2052
Information
- Symbol
- LINC02052
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 2052
- Entrez Gene ID
- 253573
- Genome
- hg19
- Position
- chr3:186,172,780-186,211,450
- Genome
- hg38
- Position
- chr3:186,454,991-186,493,661
- HGNC
- HGNC:27372 HGNC
- Ensembl
- ENSG00000224406 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely pathogenic | 1 | 0 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
0 |
 |
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
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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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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| Category | : |
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| 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 | : |
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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 | |||||||||||||||
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000664567.1 | hg38 | chr3 | 186,454,989 | 186,458,472 | 3,484 |
| ENST00000669782.1 | hg38 | chr3 | 186,454,987 | 186,458,460 | 3,474 |
| ENST00000664591.1 | hg38 | chr3 | 186,455,010 | 186,458,467 | 3,458 |
| ENST00000654350.1 | hg38 | chr3 | 186,466,201 | 186,492,965 | 26,765 |
| ENST00000427914.5 | hg38 | chr3 | 186,454,991 | 186,493,661 | 38,671 |
| ENST00000669782.1 | hg19 | chr3 | 186,172,776 | 186,176,249 | 3,474 |
| ENST00000664567.1 | hg19 | chr3 | 186,172,778 | 186,176,261 | 3,484 |
| ENST00000427914.5 | hg19 | chr3 | 186,172,780 | 186,211,450 | 38,671 |
| ENST00000664591.1 | hg19 | chr3 | 186,172,799 | 186,176,256 | 3,458 |
| ENST00000654350.1 | hg19 | chr3 | 186,183,990 | 186,210,754 | 26,765 |
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