CDK16 cyclin dependent kinase 16

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: CDK16
Type: protein-coding
Description: cyclin dependent kinase 16
Entrez Gene ID: 5127
Genome: hg19
Position: chrX:47,082,417-47,089,392
Genome: hg38
Position: chrX:47,223,018-47,229,993
MIM: 311550 OMIM
HGNC: HGNC:8749 HGNC
Ensembl: ENSG00000102225 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	16
Likely benign	0	8
not provided	6	0
Uncertain significance	0	60

Ranking

	ClinVar
	0
	0
	6
	76
	2

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

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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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	PCTAIRE
SYNONYM	PCTAIRE1
SYNONYM	PCTGAIRE
SYNONYM	PCTK1
MIM	311550 OMIM
HGNC	HGNC:8749 HGNC
Ensembl	ENSG00000102225 Ensembl
AllianceGenome	HGNC:8749

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000518022.5	hg38	chrX	47,223,009	47,228,990	5,982
ENST00000457458.6	hg38	chrX	47,218,233	47,229,997	11,765
ENST00000276052.10	hg38	chrX	47,223,018	47,229,993	6,976
ENST00000357227.9	hg38	chrX	47,218,681	47,229,997	11,317
ENST00000457458.6	hg19	chrX	47,077,632	47,089,396	11,765
ENST00000357227.9	hg19	chrX	47,078,080	47,089,396	11,317
ENST00000276052.10	hg19	chrX	47,082,417	47,089,392	6,976
ENST00000518022.5	hg19	chrX	47,082,408	47,088,389	5,982

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