APCDD1L-DT APCDD1L divergent transcript
Information
- Symbol
- APCDD1L-DT
- Type
- ncRNA
- Description
- APCDD1L divergent transcript
- Entrez Gene ID
- 149773
- Genome
- hg19
- Position
- chr20:57,090,589-57,150,487
- Genome
- hg38
- Position
- chr20:58,515,533-58,575,431
- HGNC
- HGNC:27152 HGNC
- Ensembl
- ENSG00000231290 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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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 | APCDD1L-AS1 |
HGNC | HGNC:27152 HGNC |
Ensembl | ENSG00000231290 Ensembl |
AllianceGenome | HGNC:27152 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000420279.5 | hg38 | chr20 | 58,515,499 | 58,547,822 | 32,324 |
ENST00000439558.5 | hg38 | chr20 | 58,515,727 | 58,573,970 | 58,244 |
ENST00000445984.5 | hg38 | chr20 | 58,515,499 | 58,523,802 | 8,304 |
ENST00000661476.1 | hg38 | chr20 | 58,515,533 | 58,575,431 | 59,899 |
ENST00000424205.1 | hg38 | chr20 | 58,523,160 | 58,573,824 | 50,665 |
ENST00000448374.5 | hg38 | chr20 | 58,515,499 | 58,524,728 | 9,230 |
ENST00000701694.1 | hg38 | chr20 | 58,515,499 | 58,606,995 | 91,497 |
ENST00000427794.1 | hg38 | chr20 | 58,515,568 | 58,522,492 | 6,925 |
ENST00000427140.5 | hg38 | chr20 | 58,515,379 | 58,619,888 | 104,510 |
ENST00000427140.5 | hg19 | chr20 | 57,090,435 | 57,194,944 | 104,510 |
ENST00000445984.5 | hg19 | chr20 | 57,090,555 | 57,098,858 | 8,304 |
ENST00000448374.5 | hg19 | chr20 | 57,090,555 | 57,099,784 | 9,230 |
ENST00000420279.5 | hg19 | chr20 | 57,090,555 | 57,122,878 | 32,324 |
ENST00000701694.1 | hg19 | chr20 | 57,090,555 | 57,182,051 | 91,497 |
ENST00000661476.1 | hg19 | chr20 | 57,090,589 | 57,150,487 | 59,899 |
ENST00000427794.1 | hg19 | chr20 | 57,090,624 | 57,097,548 | 6,925 |
ENST00000439558.5 | hg19 | chr20 | 57,090,783 | 57,149,026 | 58,244 |
ENST00000424205.1 | hg19 | chr20 | 57,098,216 | 57,148,880 | 50,665 |
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