PEX11A peroxisomal biogenesis factor 11 alpha

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Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: PEX11A
Type: protein-coding
Description: peroxisomal biogenesis factor 11 alpha
Entrez Gene ID: 8800
Genome: hg19
Position: chr15:90,224,766-90,233,985
Genome: hg38
Position: chr15:89,681,535-89,690,754
MIM: 603866 OMIM
HGNC: HGNC:8852 HGNC
Ensembl: ENSG00000166821 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Likely benign	0	8
Uncertain significance	0	52

Ranking

	ClinVar
	0
	0
	0
	60
	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

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	PEX11-ALPHA
SYNONYM	PEX11alpha
SYNONYM	PMP28
SYNONYM	hsPEX11p
MIM	603866 OMIM
HGNC	HGNC:8852 HGNC
Ensembl	ENSG00000166821 Ensembl
AllianceGenome	HGNC:8852

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000561224.5	hg38	chr15	89,681,305	89,690,753	9,449
ENST00000300056.8	hg38	chr15	89,681,535	89,690,754	9,220
ENST00000559170.1	hg38	chr15	89,683,251	89,690,783	7,533
ENST00000561257.1	hg38	chr15	89,683,080	89,690,662	7,583
ENST00000561224.5	hg19	chr15	90,224,536	90,233,984	9,449
ENST00000300056.8	hg19	chr15	90,224,766	90,233,985	9,220
ENST00000561257.1	hg19	chr15	90,226,311	90,233,893	7,583
ENST00000559170.1	hg19	chr15	90,226,482	90,234,014	7,533

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