LINC02037 long intergenic non-protein coding RNA 2037
Information
- Symbol
- LINC02037
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 2037
- Entrez Gene ID
- 101929337
- Genome
- hg19
- Position
- chr3:193,965,427-193,976,605
- Genome
- hg38
- Position
- chr3:194,247,638-194,258,816
- HGNC
- HGNC:52877 HGNC
- Ensembl
- ENSG00000238097 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 |
---|---|---|---|---|---|
ENST00000664340.1 | hg38 | chr3 | 194,247,638 | 194,258,816 | 11,179 |
ENST00000691562.1 | hg38 | chr3 | 194,247,647 | 194,260,713 | 13,067 |
ENST00000693372.1 | hg38 | chr3 | 194,247,646 | 194,257,067 | 9,422 |
ENST00000664340.1 | hg19 | chr3 | 193,965,427 | 193,976,605 | 11,179 |
ENST00000693372.1 | hg19 | chr3 | 193,965,435 | 193,974,856 | 9,422 |
ENST00000691562.1 | hg19 | chr3 | 193,965,436 | 193,978,502 | 13,067 |
Genome browser