EPM2A-DT EPM2A divergent transcript
Information
- Symbol
- EPM2A-DT
- Type
- ncRNA
- Description
- EPM2A divergent transcript
- Entrez Gene ID
- 100507557
- Genome
- hg19
- Position
- chr6:146,135,998-146,208,555
- Genome
- hg38
- Position
- chr6:145,814,862-145,887,419
- HGNC
- HGNC:48990 HGNC
- Ensembl
- ENSG00000235652 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 | FBXO30-DT |
HGNC | HGNC:48990 HGNC |
Ensembl | ENSG00000235652 Ensembl |
AllianceGenome | HGNC:48990 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000663890.1 | hg38 | chr6 | 145,814,862 | 145,887,419 | 72,558 |
ENST00000658327.1 | hg38 | chr6 | 145,814,895 | 145,873,177 | 58,283 |
ENST00000452617.7 | hg38 | chr6 | 145,814,873 | 145,885,835 | 70,963 |
ENST00000690526.1 | hg38 | chr6 | 145,814,909 | 145,884,717 | 69,809 |
ENST00000691670.1 | hg38 | chr6 | 145,814,891 | 145,883,307 | 68,417 |
ENST00000452617.7 | hg19 | chr6 | 146,136,009 | 146,206,971 | 70,963 |
ENST00000691670.1 | hg19 | chr6 | 146,136,027 | 146,204,443 | 68,417 |
ENST00000658327.1 | hg19 | chr6 | 146,136,031 | 146,194,313 | 58,283 |
ENST00000663890.1 | hg19 | chr6 | 146,135,998 | 146,208,555 | 72,558 |
ENST00000690526.1 | hg19 | chr6 | 146,136,045 | 146,205,853 | 69,809 |
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