TRIM66 tripartite motif containing 66

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: TRIM66
Type: protein-coding
Description: tripartite motif containing 66
Entrez Gene ID: 9866
Genome: hg19
Position: chr11:8,633,587-8,704,212
Genome: hg38
Position: chr11:8,612,040-8,682,665
MIM: 612000 OMIM
HGNC: HGNC:29005 HGNC
Ensembl: ENSG00000166436 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	8
Likely benign	0	12
Conflicting classifications of pathogenicity	0	2
Uncertain significance	0	144

Ranking

	ClinVar
	0
	0
	0
	164
	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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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	C11orf29
SYNONYM	TIF1D
SYNONYM	TIF1DELTA
MIM	612000 OMIM
HGNC	HGNC:29005 HGNC
Ensembl	ENSG00000166436 Ensembl
AllianceGenome	HGNC:29005

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000525788.2	hg38	chr11	8,612,037	8,658,580	46,544
ENST00000705689.1	hg38	chr11	8,612,040	8,682,632	70,593
ENST00000705690.1	hg38	chr11	8,615,539	8,658,836	43,298
ENST00000646038.2	hg38	chr11	8,612,040	8,682,665	70,626
ENST00000525788.2	hg19	chr11	8,633,584	8,680,127	46,544
ENST00000705689.1	hg19	chr11	8,633,587	8,704,179	70,593
ENST00000646038.2	hg19	chr11	8,633,587	8,704,212	70,626
ENST00000705690.1	hg19	chr11	8,637,086	8,680,383	43,298

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