LINC02762 long intergenic non-protein coding RNA 2762
Information
- Symbol
- LINC02762
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 2762
- Entrez Gene ID
- 283140
- Genome
- hg19
- Position
- chr11:112,160,947-112,164,839
- Genome
- hg38
- Position
- chr11:112,290,224-112,294,116
- HGNC
- HGNC:27443 HGNC
- Ensembl
- ENSG00000250303 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
|
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 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000693507.1 | hg38 | chr11 | 112,290,224 | 112,294,116 | 3,893 |
ENST00000504610.2 | hg38 | chr11 | 112,270,749 | 112,362,534 | 91,786 |
ENST00000529938.2 | hg38 | chr11 | 112,290,218 | 112,294,092 | 3,875 |
ENST00000419895.5 | hg38 | chr11 | 112,290,201 | 112,294,119 | 3,919 |
ENST00000689463.1 | hg38 | chr11 | 112,290,273 | 112,294,116 | 3,844 |
ENST00000532168.3 | hg38 | chr11 | 112,270,748 | 112,291,776 | 21,029 |
ENST00000532168.3 | hg19 | chr11 | 112,141,471 | 112,162,499 | 21,029 |
ENST00000504610.2 | hg19 | chr11 | 112,141,472 | 112,233,257 | 91,786 |
ENST00000419895.5 | hg19 | chr11 | 112,160,924 | 112,164,842 | 3,919 |
ENST00000529938.2 | hg19 | chr11 | 112,160,941 | 112,164,815 | 3,875 |
ENST00000693507.1 | hg19 | chr11 | 112,160,947 | 112,164,839 | 3,893 |
ENST00000689463.1 | hg19 | chr11 | 112,160,996 | 112,164,839 | 3,844 |
Genome browser