ARID5B AT-rich interaction domain 5B

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: ARID5B
Type: protein-coding
Description: AT-rich interaction domain 5B
Entrez Gene ID: 84159
Genome: hg19
Position: chr10:63,661,458-63,856,703
Genome: hg38
Position: chr10:61,901,699-62,096,944
MIM: 608538 OMIM
HGNC: HGNC:17362 HGNC
Ensembl: ENSG00000150347 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	10
Likely benign	0	24
not provided	21	0
Uncertain significance	0	100

Ranking

	ClinVar
	0
	0
	2
	132
	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

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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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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	DESRT
SYNONYM	MRF-2
SYNONYM	MRF2
MIM	608538 OMIM
HGNC	HGNC:17362 HGNC
Ensembl	ENSG00000150347 Ensembl
AllianceGenome	HGNC:17362

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000681100.1	hg38	chr10	61,901,699	62,096,944	195,246
ENST00000644638.1	hg38	chr10	61,901,684	62,025,352	123,669
ENST00000309334.5	hg38	chr10	62,049,211	62,093,064	43,854
ENST00000279873.12	hg38	chr10	61,901,699	62,096,944	195,246
ENST00000644638.1	hg19	chr10	63,661,443	63,785,111	123,669
ENST00000681100.1	hg19	chr10	63,661,458	63,856,703	195,246
ENST00000279873.12	hg19	chr10	63,661,458	63,856,703	195,246
ENST00000309334.5	hg19	chr10	63,808,970	63,852,823	43,854

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