GMNN geminin DNA replication inhibitor

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Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: GMNN
Type: protein-coding
Description: geminin DNA replication inhibitor
Entrez Gene ID: 51053
Genome: hg19
Position: chr6:24,775,165-24,786,327
Genome: hg38
Position: chr6:24,774,937-24,786,099
MIM: 602842 OMIM
HGNC: HGNC:17493 HGNC
Ensembl: ENSG00000112312 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Pathogenic	0	4
Likely pathogenic	0	2
Benign	0	40
Likely benign	0	52
Conflicting classifications of pathogenicity	0	6
Uncertain significance	0	68

Ranking

	ClinVar
	0
	0
	14
	152
	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

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	:
Search word	:
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	Gem
SYNONYM	MGORS6
MIM	602842 OMIM
HGNC	HGNC:17493 HGNC
Ensembl	ENSG00000112312 Ensembl
AllianceGenome	HGNC:17493

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000620958.4	hg38	chr6	24,775,413	24,786,093	10,681
ENST00000356509.7	hg38	chr6	24,774,931	24,786,095	11,165
ENST00000230056.8	hg38	chr6	24,774,937	24,786,099	11,163
ENST00000356509.7	hg19	chr6	24,775,159	24,786,323	11,165
ENST00000230056.8	hg19	chr6	24,775,165	24,786,327	11,163
ENST00000620958.4	hg19	chr6	24,775,641	24,786,321	10,681

Key	Value
strand	+
start	24,775,158
Gene Symbol	GMNN
Entrez GeneId	51,053
Chr Band	6p22.3
end	24,786,324
chr	chr6

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