LINC01089 long intergenic non-protein coding RNA 1089
Information
- Symbol
- LINC01089
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 1089
- Entrez Gene ID
- 338799
- Genome
- hg19
- Position
- chr12:122,233,173-122,241,390
- Genome
- hg38
- Position
- chr12:121,795,267-121,803,484
- HGNC
- HGNC:27886 HGNC
- Ensembl
- ENSG00000212694 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 |
|---|---|---|---|---|---|
| ENST00000542933.5 | hg38 | chr12 | 121,795,267 | 121,802,910 | 7,644 |
| ENST00000429892.5 | hg38 | chr12 | 121,795,267 | 121,803,484 | 8,218 |
| ENST00000536662.5 | hg38 | chr12 | 121,799,553 | 121,802,945 | 3,393 |
| ENST00000543334.5 | hg38 | chr12 | 121,799,384 | 121,802,604 | 3,221 |
| ENST00000538335.1 | hg38 | chr12 | 121,799,849 | 121,803,906 | 4,058 |
| ENST00000542933.5 | hg19 | chr12 | 122,233,173 | 122,240,816 | 7,644 |
| ENST00000429892.5 | hg19 | chr12 | 122,233,173 | 122,241,390 | 8,218 |
| ENST00000543334.5 | hg19 | chr12 | 122,237,290 | 122,240,510 | 3,221 |
| ENST00000536662.5 | hg19 | chr12 | 122,237,459 | 122,240,851 | 3,393 |
| ENST00000538335.1 | hg19 | chr12 | 122,237,755 | 122,241,812 | 4,058 |
Genome browser