LINC01255 long intergenic non-protein coding RNA 1255
Information
- Symbol
- LINC01255
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 1255
- Entrez Gene ID
- 101927433
- Genome
- hg19
- Position
- chr18:11,490,051-11,491,779
- Genome
- hg38
- Position
- chr18:11,490,052-11,491,780
- HGNC
- HGNC:49871 HGNC
- Ensembl
- ENSG00000267252 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 |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
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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Filtering | : |
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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000655180.1 | hg38 | chr18 | 11,490,065 | 11,491,780 | 1,716 |
ENST00000661916.1 | hg38 | chr18 | 11,490,077 | 11,491,798 | 1,722 |
ENST00000656361.1 | hg38 | chr18 | 11,487,362 | 11,488,963 | 1,602 |
ENST00000665603.1 | hg38 | chr18 | 11,490,029 | 11,497,310 | 7,282 |
ENST00000661687.1 | hg38 | chr18 | 11,490,028 | 11,523,087 | 33,060 |
ENST00000659512.1 | hg38 | chr18 | 11,486,205 | 11,507,234 | 21,030 |
ENST00000654285.1 | hg38 | chr18 | 11,490,047 | 11,506,981 | 16,935 |
ENST00000657252.1 | hg38 | chr18 | 11,490,052 | 11,491,780 | 1,729 |
ENST00000670553.1 | hg38 | chr18 | 11,490,040 | 11,506,964 | 16,925 |
ENST00000654376.1 | hg38 | chr18 | 11,490,042 | 11,506,983 | 16,942 |
ENST00000658793.1 | hg38 | chr18 | 11,490,068 | 11,492,113 | 2,046 |
ENST00000666178.1 | hg38 | chr18 | 11,490,083 | 11,506,978 | 16,896 |
ENST00000655180.1 | hg19 | chr18 | 11,490,064 | 11,491,779 | 1,716 |
ENST00000659512.1 | hg19 | chr18 | 11,486,204 | 11,507,233 | 21,030 |
ENST00000654285.1 | hg19 | chr18 | 11,490,046 | 11,506,980 | 16,935 |
ENST00000654376.1 | hg19 | chr18 | 11,490,041 | 11,506,982 | 16,942 |
ENST00000657252.1 | hg19 | chr18 | 11,490,051 | 11,491,779 | 1,729 |
ENST00000656361.1 | hg19 | chr18 | 11,487,361 | 11,488,962 | 1,602 |
ENST00000661687.1 | hg19 | chr18 | 11,490,027 | 11,523,086 | 33,060 |
ENST00000665603.1 | hg19 | chr18 | 11,490,028 | 11,497,309 | 7,282 |
ENST00000670553.1 | hg19 | chr18 | 11,490,039 | 11,506,963 | 16,925 |
ENST00000658793.1 | hg19 | chr18 | 11,490,067 | 11,492,112 | 2,046 |
ENST00000661916.1 | hg19 | chr18 | 11,490,076 | 11,491,797 | 1,722 |
ENST00000666178.1 | hg19 | chr18 | 11,490,082 | 11,506,977 | 16,896 |
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