MLLT1 MLLT1 super elongation complex subunit
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 0 | 2 |
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 30 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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34 |
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2 |
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 |
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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 |
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 | ENL |
SYNONYM | LTG19 |
SYNONYM | YEATS1 |
MIM | 159556 OMIM |
HGNC | HGNC:7134 HGNC |
Ensembl | ENSG00000130382 Ensembl |
AllianceGenome | HGNC:7134 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000585588.2 | hg38 | chr19 | 6,212,465 | 6,217,057 | 4,593 |
ENST00000252674.9 | hg38 | chr19 | 6,210,381 | 6,279,975 | 69,595 |
ENST00000252674.9 | hg19 | chr19 | 6,210,392 | 6,279,986 | 69,595 |
ENST00000585588.2 | hg19 | chr19 | 6,212,476 | 6,217,068 | 4,593 |
Key | Value |
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strand | - |
UniProt | OG |
start | 6,210,391 |
Gene Symbol | MLLT1 |
Entrez GeneId | 4,298 |
Chr Band | 19p13.3 |
end | 6,279,958 |
chr | chr19 |
Name | myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 1 (ENL) |
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