DDX11-AS1 DDX11 antisense RNA 1
Information
- Symbol
- DDX11-AS1
- Type
- ncRNA
- Description
- DDX11 antisense RNA 1
- Entrez Gene ID
- 100506660
- Genome
- hg19
- Position
- chr12:31,172,368-31,226,720
- Genome
- hg38
- Position
- chr12:31,019,434-31,073,786
- HGNC
- HGNC:44176 HGNC
- Ensembl
- ENSG00000245614 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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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 | CONCR |
SYNONYM | SCAT4 |
HGNC | HGNC:44176 HGNC |
Ensembl | ENSG00000245614 Ensembl |
AllianceGenome | HGNC:44176 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000669174.1 | hg38 | chr12 | 31,019,434 | 31,073,786 | 54,353 |
ENST00000701923.1 | hg38 | chr12 | 31,056,204 | 31,073,807 | 17,604 |
ENST00000669174.1 | hg19 | chr12 | 31,172,368 | 31,226,720 | 54,353 |
ENST00000701923.1 | hg19 | chr12 | 31,209,138 | 31,226,741 | 17,604 |
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