PHF11 PHD finger protein 11

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: PHF11
Type: protein-coding
Description: PHD finger protein 11
Entrez Gene ID: 51131
Genome: hg19
Position: chr13:50,070,089-50,103,112
Genome: hg38
Position: chr13:49,495,953-49,528,976
MIM: 607796 OMIM
HGNC: HGNC:17024 HGNC
Ensembl: ENSG00000136147 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	4
Likely benign	0	6
Uncertain significance	0	32

Ranking

	ClinVar
	0
	0
	0
	42
	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

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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Filtering	:

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	APY
SYNONYM	BCAP
SYNONYM	IGEL
SYNONYM	IGER
SYNONYM	IGHER
SYNONYM	NY-REN-34
SYNONYM	NYREN34
MIM	607796 OMIM
HGNC	HGNC:17024 HGNC
Ensembl	ENSG00000136147 Ensembl
AllianceGenome	HGNC:17024

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000378319.8	hg38	chr13	49,495,953	49,528,976	33,024
ENST00000488958.5	hg38	chr13	49,497,113	49,528,976	31,864
ENST00000357596.7	hg38	chr13	49,496,392	49,528,981	32,590
ENST00000496623.5	hg38	chr13	49,495,970	49,518,834	22,865
ENST00000357596.7	hg19	chr13	50,070,528	50,103,117	32,590
ENST00000378319.8	hg19	chr13	50,070,089	50,103,112	33,024
ENST00000496623.5	hg19	chr13	50,070,106	50,092,970	22,865
ENST00000488958.5	hg19	chr13	50,071,249	50,103,112	31,864

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