LINC01234 long intergenic non-protein coding RNA 1234
Information
- Symbol
- LINC01234
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 1234
- Entrez Gene ID
- 100506465
- Genome
- hg19
- Position
- chr12:114,181,245-114,211,531
- Genome
- hg38
- Position
- chr12:113,743,440-113,773,726
- HGNC
- HGNC:49757 HGNC
- Ensembl
- ENSG00000249550 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 | LCAL84 |
| SYNONYM | MBOP |
| SYNONYM | onco-lncRNA-32 |
| HGNC | HGNC:49757 HGNC |
| Ensembl | ENSG00000249550 Ensembl |
| AllianceGenome | HGNC:49757 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000662465.1 | hg38 | chr12 | 113,743,657 | 113,773,686 | 30,030 |
| ENST00000510694.3 | hg38 | chr12 | 113,751,014 | 113,773,708 | 22,695 |
| ENST00000655514.1 | hg38 | chr12 | 113,743,440 | 113,773,726 | 30,287 |
| ENST00000669504.1 | hg38 | chr12 | 113,704,966 | 113,773,699 | 68,734 |
| ENST00000661760.1 | hg38 | chr12 | 113,583,886 | 113,773,686 | 189,801 |
| ENST00000661760.1 | hg19 | chr12 | 114,021,691 | 114,211,491 | 189,801 |
| ENST00000510694.3 | hg19 | chr12 | 114,188,819 | 114,211,513 | 22,695 |
| ENST00000655514.1 | hg19 | chr12 | 114,181,245 | 114,211,531 | 30,287 |
| ENST00000662465.1 | hg19 | chr12 | 114,181,462 | 114,211,491 | 30,030 |
| ENST00000669504.1 | hg19 | chr12 | 114,142,771 | 114,211,504 | 68,734 |
Genome browser