DLEU1 deleted in lymphocytic leukemia 1
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.]
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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 |
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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 |
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Target data | : |
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 | BCMS |
SYNONYM | BCMS1 |
SYNONYM | DLB1 |
SYNONYM | DLEU2 |
SYNONYM | LEU1 |
SYNONYM | LEU2 |
SYNONYM | LINC00021 |
SYNONYM | NCRNA00021 |
SYNONYM | XTP6 |
MIM | 605765 OMIM |
HGNC | HGNC:13747 HGNC |
Ensembl | ENSG00000176124 Ensembl |
AllianceGenome | HGNC:13747 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000413510.4 | hg38 | chr13 | 50,807,855 | 50,849,905 | 42,051 |
ENST00000668174.1 | hg38 | chr13 | 50,719,188 | 50,724,541 | 5,354 |
ENST00000647700.1 | hg38 | chr13 | 50,397,419 | 50,654,079 | 256,661 |
ENST00000671384.1 | hg38 | chr13 | 50,713,179 | 50,716,985 | 3,807 |
ENST00000652753.1 | hg38 | chr13 | 50,678,157 | 50,906,856 | 228,700 |
ENST00000484869.6 | hg38 | chr13 | 50,401,226 | 50,631,599 | 230,374 |
ENST00000650910.1 | hg38 | chr13 | 50,677,957 | 50,722,427 | 44,471 |
ENST00000469754.3 | hg38 | chr13 | 50,082,169 | 50,107,218 | 25,050 |
ENST00000491615.5 | hg38 | chr13 | 50,082,171 | 50,528,534 | 446,364 |
ENST00000473075.3 | hg38 | chr13 | 50,221,273 | 50,401,366 | 180,094 |
ENST00000469095.6 | hg38 | chr13 | 50,401,226 | 50,528,643 | 127,418 |
ENST00000658634.1 | hg38 | chr13 | 50,678,273 | 50,726,489 | 48,217 |
ENST00000469754.3 | hg19 | chr13 | 50,656,305 | 50,681,354 | 25,050 |
ENST00000413510.4 | hg19 | chr13 | 51,381,991 | 51,424,041 | 42,051 |
ENST00000469095.6 | hg19 | chr13 | 50,975,362 | 51,102,779 | 127,418 |
ENST00000491615.5 | hg19 | chr13 | 50,656,307 | 51,102,670 | 446,364 |
ENST00000484869.6 | hg19 | chr13 | 50,975,362 | 51,205,735 | 230,374 |
ENST00000473075.3 | hg19 | chr13 | 50,795,409 | 50,975,502 | 180,094 |
ENST00000647700.1 | hg19 | chr13 | 50,971,555 | 51,228,215 | 256,661 |
ENST00000650910.1 | hg19 | chr13 | 51,252,093 | 51,296,563 | 44,471 |
ENST00000652753.1 | hg19 | chr13 | 51,252,293 | 51,480,992 | 228,700 |
ENST00000658634.1 | hg19 | chr13 | 51,252,409 | 51,300,625 | 48,217 |
ENST00000671384.1 | hg19 | chr13 | 51,287,315 | 51,291,121 | 3,807 |
ENST00000668174.1 | hg19 | chr13 | 51,293,324 | 51,298,677 | 5,354 |
Key | Value |
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strand | + |
UniProt | TSG |
start | 50,656,304 |
Gene Symbol | DLEU1 |
Entrez GeneId | 10,301 |
Chr Band | 13q14.3 |
end | 51,102,778 |
chr | chr13 |
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