LINC02371 long intergenic non-protein coding RNA 2371
Information
- Symbol
- LINC02371
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 2371
- Entrez Gene ID
- 107984539
- Genome
- hg19
- Position
- chr12:2,849,198-2,854,685
- Genome
- hg38
- Position
- chr12:2,740,032-2,745,519
- HGNC
- HGNC:53293 HGNC
- Ensembl
- ENSG00000274659 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 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
|
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 |
---|---|---|---|---|---|
ENST00000613818.4 | hg38 | chr12 | 2,740,032 | 2,745,519 | 5,488 |
ENST00000670289.3 | hg38 | chr12 | 2,740,032 | 2,746,665 | 6,634 |
ENST00000686731.2 | hg38 | chr12 | 2,740,066 | 2,744,364 | 4,299 |
ENST00000701181.1 | hg38 | chr12 | 2,740,075 | 2,744,080 | 4,006 |
ENST00000613818.4 | hg19 | chr12 | 2,849,198 | 2,854,685 | 5,488 |
ENST00000670289.3 | hg19 | chr12 | 2,849,198 | 2,855,831 | 6,634 |
ENST00000686731.2 | hg19 | chr12 | 2,849,232 | 2,853,530 | 4,299 |
ENST00000701181.1 | hg19 | chr12 | 2,849,241 | 2,853,246 | 4,006 |
Genome browser