SPIN2B spindlin family member 2B

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Clinical Significance
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Frequency
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Information

Symbol: SPIN2B
Type: protein-coding
Description: spindlin family member 2B
Entrez Gene ID: 474343
Genome: hg19
Position: chrX:57,146,115-57,147,981
Genome: hg38
Position: chrX:57,119,682-57,121,548
MIM: 300517 OMIM
HGNC: HGNC:33147 HGNC
Ensembl: ENSG00000186787 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Likely benign	0	2
not provided	6	0
Uncertain significance	0	4

Ranking

	ClinVar
	0
	0
	0
	6
	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

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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
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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	SPIN-2
SYNONYM	SPIN-2B
SYNONYM	SPIN2_duplicate
SYNONYM	TDRD26
SYNONYM	dJ323P24.2
MIM	300517 OMIM
HGNC	HGNC:33147 HGNC
Ensembl	ENSG00000186787 Ensembl
AllianceGenome	HGNC:33147

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000275988.5	hg38	chrX	57,119,682	57,121,491	1,810
ENST00000434397.3	hg38	chrX	57,119,682	57,121,548	1,867
ENST00000333933.3	hg38	chrX	57,119,683	57,121,546	1,864
ENST00000374910.3	hg38	chrX	57,119,682	57,121,315	1,634
ENST00000374910.3	hg19	chrX	57,146,115	57,147,748	1,634
ENST00000275988.5	hg19	chrX	57,146,115	57,147,924	1,810
ENST00000434397.3	hg19	chrX	57,146,115	57,147,981	1,867
ENST00000333933.3	hg19	chrX	57,146,116	57,147,979	1,864

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