LINC00665 long intergenic non-protein coding RNA 665
Information
- Symbol
- LINC00665
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 665
- Entrez Gene ID
- 100506930
- Genome
- hg19
- Position
- chr19:36,803,969-36,822,663
- Genome
- hg38
- Position
- chr19:36,313,067-36,331,761
- HGNC
- HGNC:44323 HGNC
- Ensembl
- ENSG00000232677 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 |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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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Search word | : | |
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 |
Type | ID |
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SYNONYM | CIP2A-BP |
HGNC | HGNC:44323 HGNC |
Ensembl | ENSG00000232677 Ensembl |
AllianceGenome | HGNC:44323 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000658991.1 | hg38 | chr19 | 36,324,926 | 36,331,734 | 6,809 |
ENST00000676298.1 | hg38 | chr19 | 36,320,572 | 36,331,731 | 11,160 |
ENST00000675167.1 | hg38 | chr19 | 36,316,039 | 36,331,710 | 15,672 |
ENST00000676422.1 | hg38 | chr19 | 36,259,540 | 36,264,788 | 5,249 |
ENST00000590657.2 | hg38 | chr19 | 36,315,035 | 36,331,634 | 16,600 |
ENST00000675324.1 | hg38 | chr19 | 36,262,260 | 36,321,324 | 59,065 |
ENST00000675074.1 | hg38 | chr19 | 36,326,954 | 36,331,701 | 4,748 |
ENST00000666182.4 | hg38 | chr19 | 36,313,067 | 36,331,761 | 18,695 |
ENST00000658042.1 | hg38 | chr19 | 36,315,174 | 36,331,699 | 16,526 |
ENST00000656137.1 | hg38 | chr19 | 36,324,924 | 36,331,739 | 6,816 |
ENST00000438368.7 | hg38 | chr19 | 36,319,711 | 36,331,708 | 11,998 |
ENST00000658301.1 | hg38 | chr19 | 36,324,924 | 36,330,492 | 5,569 |
ENST00000590657.2 | hg19 | chr19 | 36,805,937 | 36,822,536 | 16,600 |
ENST00000658042.1 | hg19 | chr19 | 36,806,076 | 36,822,601 | 16,526 |
ENST00000438368.7 | hg19 | chr19 | 36,810,613 | 36,822,610 | 11,998 |
ENST00000658301.1 | hg19 | chr19 | 36,815,826 | 36,821,394 | 5,569 |
ENST00000656137.1 | hg19 | chr19 | 36,815,826 | 36,822,641 | 6,816 |
ENST00000658991.1 | hg19 | chr19 | 36,815,828 | 36,822,636 | 6,809 |
ENST00000675074.1 | hg19 | chr19 | 36,817,856 | 36,822,603 | 4,748 |
ENST00000676422.1 | hg19 | chr19 | 36,750,442 | 36,755,690 | 5,249 |
ENST00000666182.4 | hg19 | chr19 | 36,803,969 | 36,822,663 | 18,695 |
ENST00000675167.1 | hg19 | chr19 | 36,806,941 | 36,822,612 | 15,672 |
ENST00000675324.1 | hg19 | chr19 | 36,753,162 | 36,812,226 | 59,065 |
ENST00000676298.1 | hg19 | chr19 | 36,811,474 | 36,822,633 | 11,160 |
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