SUMO3 small ubiquitin like modifier 3

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: SUMO3
Type: protein-coding
Description: small ubiquitin like modifier 3
Entrez Gene ID: 6612
Genome: hg19
Position: chr21:46,225,532-46,238,044
Genome: hg38
Position: chr21:44,805,617-44,818,129
MIM: 602231 OMIM
HGNC: HGNC:11124 HGNC
Ensembl: ENSG00000184900 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	4
Likely benign	0	2
not provided	1	0
Uncertain significance	0	2

Ranking

	ClinVar
	0
	0
	0
	8
	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

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	:
Search word	:
Filtering	:

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	SMT3A
SYNONYM	SMT3H1
SYNONYM	SUMO-3
SYNONYM	Smt3B
MIM	602231 OMIM
HGNC	HGNC:11124 HGNC
Ensembl	ENSG00000184900 Ensembl
AllianceGenome	HGNC:11124

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000397898.7	hg38	chr21	44,805,617	44,818,051	12,435
ENST00000397893.3	hg38	chr21	44,808,271	44,817,968	9,698
ENST00000332859.11	hg38	chr21	44,805,617	44,818,062	12,446
ENST00000411651.6	hg38	chr21	44,805,617	44,818,129	12,513
ENST00000397898.7	hg19	chr21	46,225,532	46,237,966	12,435
ENST00000332859.11	hg19	chr21	46,225,532	46,237,977	12,446
ENST00000411651.6	hg19	chr21	46,225,532	46,238,044	12,513
ENST00000397893.3	hg19	chr21	46,228,186	46,237,883	9,698

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