CCNQ cyclin Q

Go to:

Information
Clinical Significance
Ranking
Frequency
Disease area statistics
Locus Zoom
Variants
Genome browser

Information

Symbol: CCNQ
Type: protein-coding
Description: cyclin Q
Entrez Gene ID: 92002
Genome: hg19
Position: chrX:152,853,390-152,864,573
Genome: hg38
Position: chrX:153,587,932-153,599,117
MIM: 300708 OMIM
HGNC: HGNC:28434 HGNC
Ensembl: ENSG00000262919 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Pathogenic	0	8
Likely pathogenic	0	4
Benign	0	55
Likely benign	0	30
not provided	6	0
Uncertain significance	0	22

Ranking

	ClinVar
	0
	0
	8
	99
	6

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

Search Word

Target data	:	MGeND data only
Category	:
Search word	:
Filtering	:

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
Category	:
Search word	:
Filtering	:

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	CycM
SYNONYM	FAM58A
MIM	300708 OMIM
HGNC	HGNC:28434 HGNC
Ensembl	ENSG00000262919 Ensembl
AllianceGenome	HGNC:28434

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000440428.5	hg38	chrX	153,587,932	153,599,117	11,186
ENST00000576892.8	hg38	chrX	153,587,925	153,599,139	11,215
ENST00000576892.8	hg19	chrX	152,853,383	152,864,595	11,213
ENST00000440428.5	hg19	chrX	152,853,390	152,864,573	11,184

Key	Value
strand	-
start	152,853,382
Gene Symbol	FAM58A
Entrez GeneId	92,002
Chr Band	Xq28
end	152,864,631
chr	chrX

Genome browser