SSR2 signal sequence receptor subunit 2

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: SSR2
Type: protein-coding
Description: signal sequence receptor subunit 2
Entrez Gene ID: 6746
Genome: hg19
Position: chr1:155,978,839-155,990,742
Genome: hg38
Position: chr1:156,009,048-156,020,951
MIM: 600867 OMIM
HGNC: HGNC:11324 HGNC
Ensembl: ENSG00000163479 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Uncertain significance	0	12

Ranking

	ClinVar
	0
	0
	0
	12
	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	HSD25
SYNONYM	TLAP
SYNONYM	TRAP-BETA
SYNONYM	TRAPB
MIM	600867 OMIM
HGNC	HGNC:11324 HGNC
Ensembl	ENSG00000163479 Ensembl
AllianceGenome	HGNC:11324

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000480567.5	hg38	chr1	156,009,360	156,020,889	11,530
ENST00000295702.9	hg38	chr1	156,009,048	156,020,951	11,904
ENST00000529008.5	hg38	chr1	156,009,086	156,020,917	11,832
ENST00000496742.5	hg38	chr1	156,009,105	156,020,933	11,829
ENST00000295702.9	hg19	chr1	155,978,839	155,990,742	11,904
ENST00000480567.5	hg19	chr1	155,979,151	155,990,680	11,530
ENST00000496742.5	hg19	chr1	155,978,896	155,990,724	11,829
ENST00000529008.5	hg19	chr1	155,978,877	155,990,708	11,832

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