LINC02368 long intergenic non-protein coding RNA 2368
Information
- Symbol
- LINC02368
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 2368
- Entrez Gene ID
- 101927694
- Genome
- hg19
- Position
- chr12:128,602,756-128,606,497
- Genome
- hg38
- Position
- chr12:128,118,211-128,121,952
- HGNC
- HGNC:53291 HGNC
- Ensembl
- ENSG00000256659 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 |
---|---|---|---|---|---|
ENST00000662521.1 | hg38 | chr12 | 128,118,212 | 128,123,103 | 4,892 |
ENST00000665570.1 | hg38 | chr12 | 128,116,730 | 128,121,457 | 4,728 |
ENST00000541258.2 | hg38 | chr12 | 128,118,211 | 128,121,952 | 3,742 |
ENST00000665570.1 | hg19 | chr12 | 128,601,275 | 128,606,002 | 4,728 |
ENST00000541258.2 | hg19 | chr12 | 128,602,756 | 128,606,497 | 3,742 |
ENST00000662521.1 | hg19 | chr12 | 128,602,757 | 128,607,648 | 4,892 |
Genome browser