GOLGA8B golgin A8 family member B

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: GOLGA8B
Type: protein-coding
Description: golgin A8 family member B
Entrez Gene ID: 440270
Genome: hg19
Position: chr15:34,817,296-34,875,852
Genome: hg38
Position: chr15:34,525,095-34,583,651
MIM: 609619 OMIM
HGNC: HGNC:31973 HGNC
Ensembl: ENSG00000215252 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	2
Likely benign	0	6
Uncertain significance	0	20

Ranking

	ClinVar
	0
	0
	0
	28
	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

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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	GOLGA5
MIM	609619 OMIM
HGNC	HGNC:31973 HGNC
Ensembl	ENSG00000215252 Ensembl
AllianceGenome	HGNC:31973

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000683415.1	hg38	chr15	34,525,095	34,583,651	58,557
ENST00000342314.9	hg38	chr15	34,525,207	34,536,010	10,804
ENST00000438958.2	hg38	chr15	34,525,282	34,533,260	7,979
ENST00000683415.1	hg19	chr15	34,817,296	34,875,852	58,557
ENST00000342314.9	hg19	chr15	34,817,408	34,828,211	10,804
ENST00000438958.2	hg19	chr15	34,817,483	34,825,461	7,979

Key	Value
strand	-
start	34,817,483
Gene Symbol	GOLGA8B
Entrez GeneId	440,270
Chr Band	15q14
end	34,875,770
chr	chr15

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