LINC02691 long intergenic non-protein coding RNA 2691
Information
- Symbol
- LINC02691
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 2691
- Entrez Gene ID
- 145195
- Genome
- hg19
- Position
- chr14:104,689,992-104,710,959
- Genome
- hg38
- Position
- chr14:104,223,655-104,244,622
- HGNC
- HGNC:20358 HGNC
- Ensembl
- ENSG00000258913 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
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
[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 | C14orf144 |
| HGNC | HGNC:20358 HGNC |
| Ensembl | ENSG00000258913 Ensembl |
| AllianceGenome | HGNC:20358 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000553757.1 | hg38 | chr14 | 104,223,584 | 104,288,069 | 64,486 |
| ENST00000662137.1 | hg38 | chr14 | 104,223,655 | 104,244,622 | 20,968 |
| ENST00000553757.1 | hg19 | chr14 | 104,689,921 | 104,754,406 | 64,486 |
| ENST00000662137.1 | hg19 | chr14 | 104,689,992 | 104,710,959 | 20,968 |
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