DPP4 dipeptidyl peptidase 4

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: DPP4
Type: protein-coding
Description: dipeptidyl peptidase 4
Entrez Gene ID: 1803
Genome: hg19
Position: chr2:162,848,755-162,930,725
Genome: hg38
Position: chr2:161,992,245-162,074,215
MIM: 102720 OMIM
HGNC: HGNC:3009 HGNC
Ensembl: ENSG00000197635 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	12
Likely benign	0	14
not provided	0	2
Uncertain significance	0	82

Ranking

	ClinVar
	0
	0
	0
	108
	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

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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	ADABP
SYNONYM	ADCP2
SYNONYM	CD26
SYNONYM	DPPIV
SYNONYM	TP103
MIM	102720 OMIM
HGNC	HGNC:3009 HGNC
Ensembl	ENSG00000197635 Ensembl
AllianceGenome	HGNC:3009

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000360534.8	hg38	chr2	161,992,245	162,074,215	81,971
ENST00000676768.1	hg38	chr2	161,993,609	162,074,053	80,445
ENST00000678668.1	hg38	chr2	161,992,245	162,071,190	78,946
ENST00000676810.1	hg38	chr2	161,992,245	162,074,394	82,150
ENST00000678668.1	hg19	chr2	162,848,755	162,927,700	78,946
ENST00000676768.1	hg19	chr2	162,850,119	162,930,563	80,445
ENST00000676810.1	hg19	chr2	162,848,755	162,930,904	82,150
ENST00000360534.8	hg19	chr2	162,848,755	162,930,725	81,971

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