LINC00667 long intergenic non-protein coding RNA 667
Information
- Symbol
- LINC00667
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 667
- Entrez Gene ID
- 339290
- Genome
- hg19
- Position
- chr18:5,238,157-5,246,491
- Genome
- hg38
- Position
- chr18:5,238,158-5,246,492
- HGNC
- HGNC:27906 HGNC
- Ensembl
- ENSG00000263753 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
 |
0 |
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0 |
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0 |
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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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| 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 |
|---|---|---|---|---|---|
| ENST00000580684.6 | hg38 | chr18 | 5,238,074 | 5,243,784 | 5,711 |
| ENST00000668807.1 | hg38 | chr18 | 5,238,100 | 5,245,089 | 6,990 |
| ENST00000670993.1 | hg38 | chr18 | 5,238,158 | 5,246,492 | 8,335 |
| ENST00000577439.2 | hg38 | chr18 | 5,238,780 | 5,246,508 | 7,729 |
| ENST00000666552.1 | hg38 | chr18 | 5,238,120 | 5,243,264 | 5,145 |
| ENST00000669192.1 | hg38 | chr18 | 5,238,778 | 5,243,963 | 5,186 |
| ENST00000582363.1 | hg38 | chr18 | 5,238,084 | 5,243,936 | 5,853 |
| ENST00000671289.1 | hg38 | chr18 | 5,238,158 | 5,246,494 | 8,337 |
| ENST00000665442.1 | hg38 | chr18 | 5,238,120 | 5,246,489 | 8,370 |
| ENST00000582363.1 | hg19 | chr18 | 5,238,083 | 5,243,935 | 5,853 |
| ENST00000577439.2 | hg19 | chr18 | 5,238,779 | 5,246,507 | 7,729 |
| ENST00000666552.1 | hg19 | chr18 | 5,238,119 | 5,243,263 | 5,145 |
| ENST00000580684.6 | hg19 | chr18 | 5,238,073 | 5,243,783 | 5,711 |
| ENST00000665442.1 | hg19 | chr18 | 5,238,119 | 5,246,488 | 8,370 |
| ENST00000670993.1 | hg19 | chr18 | 5,238,157 | 5,246,491 | 8,335 |
| ENST00000671289.1 | hg19 | chr18 | 5,238,157 | 5,246,493 | 8,337 |
| ENST00000668807.1 | hg19 | chr18 | 5,238,099 | 5,245,088 | 6,990 |
| ENST00000669192.1 | hg19 | chr18 | 5,238,777 | 5,243,962 | 5,186 |
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