LOHAN2 lncRNA oncogene in head and neck cancer 2
Information
- Symbol
- LOHAN2
- Type
- ncRNA
- Description
- lncRNA oncogene in head and neck cancer 2
- Entrez Gene ID
- 100506172
- Genome
- hg19
- Position
- chr16:73,420,952-73,455,293
- Genome
- hg38
- Position
- chr16:73,387,053-73,421,394
- HGNC
- HGNC:51371 HGNC
- Ensembl
- ENSG00000258779 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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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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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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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 | LINC01568 |
HGNC | HGNC:51371 HGNC |
Ensembl | ENSG00000258779 Ensembl |
AllianceGenome | HGNC:51371 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000664807.1 | hg38 | chr16 | 73,418,181 | 73,421,396 | 3,216 |
ENST00000562748.2 | hg38 | chr16 | 73,499,255 | 73,504,743 | 5,489 |
ENST00000555721.2 | hg38 | chr16 | 73,386,801 | 73,421,395 | 34,595 |
ENST00000669193.1 | hg38 | chr16 | 73,386,811 | 73,446,041 | 59,231 |
ENST00000669648.1 | hg38 | chr16 | 73,387,053 | 73,421,394 | 34,342 |
ENST00000669634.1 | hg38 | chr16 | 73,387,025 | 73,421,181 | 34,157 |
ENST00000668007.1 | hg38 | chr16 | 73,386,774 | 73,421,400 | 34,627 |
ENST00000665707.1 | hg38 | chr16 | 73,386,796 | 73,421,497 | 34,702 |
ENST00000666626.1 | hg38 | chr16 | 73,386,848 | 73,421,396 | 34,549 |
ENST00000641790.1 | hg38 | chr16 | 73,386,824 | 73,504,954 | 118,131 |
ENST00000668007.1 | hg19 | chr16 | 73,420,673 | 73,455,299 | 34,627 |
ENST00000555721.2 | hg19 | chr16 | 73,420,700 | 73,455,294 | 34,595 |
ENST00000562748.2 | hg19 | chr16 | 73,533,154 | 73,538,642 | 5,489 |
ENST00000641790.1 | hg19 | chr16 | 73,420,723 | 73,538,853 | 118,131 |
ENST00000664807.1 | hg19 | chr16 | 73,452,080 | 73,455,295 | 3,216 |
ENST00000665707.1 | hg19 | chr16 | 73,420,695 | 73,455,396 | 34,702 |
ENST00000666626.1 | hg19 | chr16 | 73,420,747 | 73,455,295 | 34,549 |
ENST00000669193.1 | hg19 | chr16 | 73,420,710 | 73,479,940 | 59,231 |
ENST00000669634.1 | hg19 | chr16 | 73,420,924 | 73,455,080 | 34,157 |
ENST00000669648.1 | hg19 | chr16 | 73,420,952 | 73,455,293 | 34,342 |
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