MLLT11 MLLT11 transcription factor 7 cofactor
Information
- Symbol
- MLLT11
- Type
- protein-coding
- Description
- MLLT11 transcription factor 7 cofactor
- Entrez Gene ID
- 10962
- Genome
- hg19
- Position
- chr1:151,032,873-151,042,020
- Genome
- hg38
- Position
- chr1:151,060,397-151,069,544
- MIM
- 604684 OMIM
- HGNC
- HGNC:16997 HGNC
- Ensembl
- ENSG00000213190 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Uncertain significance | 0 | 2 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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6 |
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0 |
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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
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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 |
---|---|
SYNONYM | AF1Q |
MIM | 604684 OMIM |
HGNC | HGNC:16997 HGNC |
Ensembl | ENSG00000213190 Ensembl |
AllianceGenome | HGNC:16997 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000368921.5 | hg38 | chr1 | 151,060,397 | 151,069,544 | 9,148 |
ENST00000368921.5 | hg19 | chr1 | 151,032,873 | 151,042,020 | 9,148 |
Key | Value |
---|---|
strand | + |
UniProt | OG |
start | 151,032,150 |
Gene Symbol | MLLT11 |
Entrez GeneId | 10,962 |
Chr Band | 1q21 |
end | 151,040,972 |
chr | chr1 |
Name | myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 11 |
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