LINC01638 long intergenic non-protein coding RNA 1638
Information
- Symbol
- LINC01638
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 1638
- Entrez Gene ID
- 105372978
- Genome
- hg19
- Position
- chr22:27,619,263-27,620,667
- Genome
- hg38
- Position
- chr22:27,223,302-27,224,706
- HGNC
- HGNC:52425 HGNC
- Ensembl
- ENSG00000233521 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
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| 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
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| 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
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| Category | : |
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| 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 | lncRNA4114 |
| HGNC | HGNC:52425 HGNC |
| Ensembl | ENSG00000233521 Ensembl |
| AllianceGenome | HGNC:52425 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000690524.1 | hg38 | chr22 | 27,223,302 | 27,224,706 | 1,405 |
| ENST00000444114.5 | hg38 | chr22 | 27,221,349 | 27,224,727 | 3,379 |
| ENST00000444114.5 | hg19 | chr22 | 27,617,310 | 27,620,688 | 3,379 |
| ENST00000690524.1 | hg19 | chr22 | 27,619,263 | 27,620,667 | 1,405 |
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