RAN RAN, member RAS oncogene family

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: RAN
Type: protein-coding
Description: RAN, member RAS oncogene family
Entrez Gene ID: 5901
Genome: hg19
Position: chr12:131,356,611-131,362,223
Genome: hg38
Position: chr12:130,872,066-130,877,678
MIM: 601179 OMIM
HGNC: HGNC:9846 HGNC
Ensembl: ENSG00000132341 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	2

Ranking

	ClinVar
	0
	0
	0
	2
	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

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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
SYNONYM	ARA24
SYNONYM	Gsp1
SYNONYM	TC4
MIM	601179 OMIM
HGNC	HGNC:9846 HGNC
Ensembl	ENSG00000132341 Ensembl
AllianceGenome	HGNC:9846

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000543796.6	hg38	chr12	130,872,066	130,877,678	5,613
ENST00000541630.5	hg38	chr12	130,872,066	130,876,733	4,668
ENST00000392369.6	hg38	chr12	130,872,070	130,876,281	4,212
ENST00000392367.4	hg38	chr12	130,872,096	130,875,963	3,868
ENST00000541679.7	hg38	chr12	130,872,082	130,876,234	4,153
ENST00000541630.5	hg19	chr12	131,356,611	131,361,278	4,668
ENST00000543796.6	hg19	chr12	131,356,611	131,362,223	5,613
ENST00000392369.6	hg19	chr12	131,356,615	131,360,826	4,212
ENST00000541679.7	hg19	chr12	131,356,627	131,360,779	4,153
ENST00000392367.4	hg19	chr12	131,356,641	131,360,508	3,868

Key	Value
strand	+
start	131,356,538
Gene Symbol	RAN
Entrez GeneId	5,901
Chr Band	12q24.3
end	131,362,222
chr	chr12

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