GTSF1 gametocyte specific factor 1

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Variants
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Information

Symbol: GTSF1
Type: protein-coding
Description: gametocyte specific factor 1
Entrez Gene ID: 121355
Genome: hg19
Position: chr12:54,849,738-54,866,411
Genome: hg38
Position: chr12:54,455,954-54,472,627
MIM: 617484 OMIM
HGNC: HGNC:26565 HGNC
Ensembl: ENSG00000170627 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	4
Uncertain significance	0	4

Ranking

	ClinVar
	0
	0
	0
	8
	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

Search Word

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	Cue110
SYNONYM	FAM112B
MIM	617484 OMIM
HGNC	HGNC:26565 HGNC
Ensembl	ENSG00000170627 Ensembl
AllianceGenome	HGNC:26565

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000305879.8	hg38	chr12	54,455,957	54,473,602	17,646
ENST00000552397.5	hg38	chr12	54,455,954	54,472,627	16,674
ENST00000552397.5	hg19	chr12	54,849,738	54,866,411	16,674
ENST00000305879.8	hg19	chr12	54,849,741	54,867,386	17,646

Key	Value
strand	-
start	54,849,735
Gene Symbol	GTSF1
Entrez GeneId	121,355
Chr Band	12q13.13
end	54,867,385
chr	chr12

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