RAI2 retinoic acid induced 2

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: RAI2
Type: protein-coding
Description: retinoic acid induced 2
Entrez Gene ID: 10742
Genome: hg19
Position: chrX:17,818,171-17,878,827
Genome: hg38
Position: chrX:17,800,051-17,860,707
MIM: 300217 OMIM
HGNC: HGNC:9835 HGNC
Ensembl: ENSG00000131831 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	10
Likely benign	0	12
not provided	7	0
Uncertain significance	0	66

Ranking

	ClinVar
	0
	0
	0
	86
	2

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

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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
MIM	300217 OMIM
HGNC	HGNC:9835 HGNC
Ensembl	ENSG00000131831 Ensembl
AllianceGenome	HGNC:9835

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000451717.6	hg38	chrX	17,800,049	17,861,298	61,250
ENST00000360011.5	hg38	chrX	17,800,051	17,860,707	60,657
ENST00000331511.5	hg38	chrX	17,800,051	17,861,236	61,186
ENST00000545871.1	hg38	chrX	17,800,051	17,861,337	61,287
ENST00000415486.7	hg38	chrX	17,800,049	17,861,298	61,250
ENST00000415486.7	hg19	chrX	17,818,169	17,879,418	61,250
ENST00000451717.6	hg19	chrX	17,818,169	17,879,418	61,250
ENST00000360011.5	hg19	chrX	17,818,171	17,878,827	60,657
ENST00000331511.5	hg19	chrX	17,818,171	17,879,356	61,186
ENST00000545871.1	hg19	chrX	17,818,171	17,879,457	61,287

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