LINC01159 long intergenic non-protein coding RNA 1159
Information
- Symbol
- LINC01159
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 1159
- Entrez Gene ID
- 102682016
- Genome
- hg19
- Position
- chr2:105,481,955-105,488,910
- Genome
- hg38
- Position
- chr2:104,865,497-104,872,452
- MIM
- 618208 OMIM
- HGNC
- HGNC:49514 HGNC
- Ensembl
- ENSG00000229743 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 | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | linc-Brn1b |
| MIM | 618208 OMIM |
| HGNC | HGNC:49514 HGNC |
| Ensembl | ENSG00000229743 Ensembl |
| AllianceGenome | HGNC:49514 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000691292.1 | hg38 | chr2 | 104,869,220 | 104,872,647 | 3,428 |
| ENST00000701008.1 | hg38 | chr2 | 104,869,220 | 104,872,598 | 3,379 |
| ENST00000454183.1 | hg38 | chr2 | 104,865,407 | 104,867,496 | 2,090 |
| ENST00000651283.1 | hg38 | chr2 | 104,865,410 | 104,868,373 | 2,964 |
| ENST00000433433.1 | hg38 | chr2 | 104,865,497 | 104,872,452 | 6,956 |
| ENST00000454183.1 | hg19 | chr2 | 105,481,865 | 105,483,954 | 2,090 |
| ENST00000651283.1 | hg19 | chr2 | 105,481,868 | 105,484,831 | 2,964 |
| ENST00000433433.1 | hg19 | chr2 | 105,481,955 | 105,488,910 | 6,956 |
| ENST00000701008.1 | hg19 | chr2 | 105,485,678 | 105,489,056 | 3,379 |
| ENST00000691292.1 | hg19 | chr2 | 105,485,678 | 105,489,105 | 3,428 |
Genome browser