DLEU2 deleted in lymphocytic leukemia 2
Clinical Significance
MGeND | ClinVar |
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Ranking
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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
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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 |
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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 |
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MGeND data only
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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 | ALT1 |
SYNONYM | BCMSUN |
SYNONYM | DLB2 |
SYNONYM | LEU2 |
SYNONYM | LINC00022 |
SYNONYM | MIR15AHG |
SYNONYM | NCRNA00022 |
SYNONYM | RFP2 |
SYNONYM | RFP2OS |
SYNONYM | TRIM13OS |
MIM | 605766 OMIM |
HGNC | HGNC:13748 HGNC |
Ensembl | ENSG00000231607 Ensembl |
AllianceGenome | HGNC:13748 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000621282.4 | hg38 | chr13 | 49,982,552 | 50,125,541 | 142,990 |
ENST00000661799.1 | hg38 | chr13 | 49,956,825 | 49,979,448 | 22,624 |
ENST00000668133.1 | hg38 | chr13 | 49,974,773 | 49,979,546 | 4,774 |
ENST00000665220.1 | hg38 | chr13 | 49,956,670 | 49,979,183 | 22,514 |
ENST00000701027.1 | hg38 | chr13 | 50,043,925 | 50,082,000 | 38,076 |
ENST00000425586.5 | hg38 | chr13 | 50,027,133 | 50,125,720 | 98,588 |
ENST00000692504.1 | hg38 | chr13 | 50,043,436 | 50,081,991 | 38,556 |
ENST00000692504.1 | hg19 | chr13 | 50,617,572 | 50,656,127 | 38,556 |
ENST00000621282.4 | hg19 | chr13 | 50,556,688 | 50,699,677 | 142,990 |
ENST00000665220.1 | hg19 | chr13 | 50,530,806 | 50,553,319 | 22,514 |
ENST00000425586.5 | hg19 | chr13 | 50,601,269 | 50,699,856 | 98,588 |
ENST00000661799.1 | hg19 | chr13 | 50,530,961 | 50,553,584 | 22,624 |
ENST00000668133.1 | hg19 | chr13 | 50,548,909 | 50,553,682 | 4,774 |
ENST00000701027.1 | hg19 | chr13 | 50,618,061 | 50,656,136 | 38,076 |
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