PPIB peptidylprolyl isomerase B

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

Symbol: PPIB
Type: protein-coding
Description: peptidylprolyl isomerase B
Entrez Gene ID: 5479
Genome: hg19
Position: chr15:64,448,016-64,455,221
Genome: hg38
Position: chr15:64,155,817-64,163,022
MIM: 123841 OMIM
HGNC: HGNC:9255 HGNC
Ensembl: ENSG00000166794 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Pathogenic	0	14
Likely pathogenic	0	16
Benign	0	26
Likely benign	0	100
Conflicting classifications of pathogenicity	0	12
not provided	0	6
Uncertain significance	0	116

Ranking

	ClinVar
	0
	0
	44
	210
	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

[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	CYP-S1
SYNONYM	CYPB
SYNONYM	HEL-S-39
SYNONYM	OI9
SYNONYM	SCYLP
MIM	123841 OMIM
HGNC	HGNC:9255 HGNC
Ensembl	ENSG00000166794 Ensembl
AllianceGenome	HGNC:9255

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000681658.1	hg38	chr15	64,155,740	64,163,026	7,287
ENST00000681397.1	hg38	chr15	64,155,740	64,163,025	7,286
ENST00000300026.4	hg38	chr15	64,155,817	64,163,022	7,206
ENST00000681397.1	hg19	chr15	64,447,939	64,455,224	7,286
ENST00000681658.1	hg19	chr15	64,447,939	64,455,225	7,287
ENST00000300026.4	hg19	chr15	64,448,016	64,455,221	7,206

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