LINC01082 long intergenic non-protein coding RNA 1082
Information
- Symbol
- LINC01082
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 1082
- Entrez Gene ID
- 100506542
- Genome
- hg19
- Position
- chr16:86,231,722-86,233,326
- Genome
- hg38
- Position
- chr16:86,198,116-86,199,720
- MIM
- 614978 OMIM
- HGNC
- HGNC:49125 HGNC
- Ensembl
- ENSG00000269186 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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0 |
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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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | TCONS_00024492 |
MIM | 614978 OMIM |
HGNC | HGNC:49125 HGNC |
Ensembl | ENSG00000269186 Ensembl |
AllianceGenome | HGNC:49125 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000669926.2 | hg38 | chr16 | 86,195,954 | 86,199,937 | 3,984 |
ENST00000650200.1 | hg38 | chr16 | 86,198,116 | 86,199,720 | 1,605 |
ENST00000669926.2 | hg19 | chr16 | 86,229,560 | 86,233,543 | 3,984 |
ENST00000650200.1 | hg19 | chr16 | 86,231,722 | 86,233,326 | 1,605 |
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