MLLT6 MLLT6, PHD finger containing

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
Locus Zoom
Variants
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Information

Symbol: MLLT6
Type: protein-coding
Description: MLLT6, PHD finger containing
Entrez Gene ID: 4302
Genome: hg19
Position: chr17:36,861,526-36,886,048
Genome: hg38
Position: chr17:38,705,273-38,729,795
MIM: 600328 OMIM
HGNC: HGNC:7138 HGNC
Ensembl: ENSG00000275023 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	4
Likely benign	0	2
Uncertain significance	0	100

Ranking

	ClinVar
	0
	0
	0
	106
	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

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
Variant name	Gene	AA change	CDS	Japanese frequency	TogoVar	Entry	Origin	Type	Annotation	Genome	Entry	Origin	Annotation	CIViC evidence	DisGeNET entry	COSMIC occurrence	Prediction

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
Name	Entry	Origin	Type	Annotation	Type	Genome	Size	Chromosome	Start	Stop	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry

Search Word

Target data	:	MGeND data only
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
Name	Entry	Origin	Type	Annotation	Type	Genome	Gene symbol	Chromosome	Genomic start	Genomic stop	Strand	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry

Type	ID
SYNONYM	AF17
MIM	600328 OMIM
HGNC	HGNC:7138 HGNC
Ensembl	ENSG00000275023 Ensembl
AllianceGenome	HGNC:7138

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000620609.4	hg38	chr17	38,705,542	38,714,756	9,215
ENST00000621332.5	hg38	chr17	38,705,273	38,729,795	24,523
ENST00000621332.5	hg19	chr17	36,861,526	36,886,048	24,523
ENST00000620609.4	hg19	chr17	36,861,795	36,871,009	9,215

Key	Value
strand	+
UniProt	OG
start	36,861,872
Gene Symbol	MLLT6
Entrez GeneId	4,302
Chr Band	17q21
end	36,886,055
chr	chr17
Name	myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 6 (AF17)

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