PRR5 proline rich 5

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: PRR5
Type: protein-coding
Description: proline rich 5
Entrez Gene ID: 55615
Genome: hg19
Position: chr22:45,072,965-45,133,561
Genome: hg38
Position: chr22:44,677,085-44,737,681
MIM: 609406 OMIM
HGNC: HGNC:31682 HGNC
Ensembl: ENSG00000186654 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Likely benign	0	4
not provided	1	2
Uncertain significance	0	54

Ranking

	ClinVar
	0
	0
	0
	58
	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

Locus Zoom

Variants

Search Word

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	FLJ20185k
SYNONYM	PP610
SYNONYM	PROTOR-1
SYNONYM	PROTOR1
MIM	609406 OMIM
HGNC	HGNC:31682 HGNC
Ensembl	ENSG00000186654 Ensembl
AllianceGenome	HGNC:31682

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000336985.11	hg38	chr22	44,702,204	44,737,681	35,478
ENST00000006251.11	hg38	chr22	44,677,057	44,737,680	60,624
ENST00000403581.5	hg38	chr22	44,677,085	44,737,681	60,597
ENST00000492475.6	hg38	chr22	44,676,981	44,737,247	60,267
ENST00000617066.4	hg38	chr22	44,668,547	44,737,681	69,135
ENST00000432186.6	hg38	chr22	44,668,713	44,737,247	68,535
ENST00000617066.4	hg19	chr22	45,064,427	45,133,561	69,135
ENST00000432186.6	hg19	chr22	45,064,593	45,133,127	68,535
ENST00000492475.6	hg19	chr22	45,072,861	45,133,127	60,267
ENST00000006251.11	hg19	chr22	45,072,937	45,133,560	60,624
ENST00000403581.5	hg19	chr22	45,072,965	45,133,561	60,597
ENST00000336985.11	hg19	chr22	45,098,084	45,133,561	35,478

Key	Value
strand	+
UniProt	TSG
start	45,064,426
Gene Symbol	PRR5
Entrez GeneId	55,615
Chr Band	22q13
end	45,133,560
chr	chr22

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