TRIM13 tripartite motif containing 13

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Variants
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Information

Symbol: TRIM13
Type: protein-coding
Description: tripartite motif containing 13
Entrez Gene ID: 10206
Genome: hg19
Position: chr13:50,571,173-50,587,316
Genome: hg38
Position: chr13:49,997,037-50,013,180
MIM: 605661 OMIM
HGNC: HGNC:9976 HGNC
Ensembl: ENSG00000204977 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Likely benign	0	4
Uncertain significance	0	42

Ranking

	ClinVar
	0
	0
	0
	46
	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
Category	:
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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	:
Search word	:
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	CAR
SYNONYM	DLEU5
SYNONYM	LEU5
SYNONYM	RFP2
SYNONYM	RNF77
MIM	605661 OMIM
HGNC	HGNC:9976 HGNC
Ensembl	ENSG00000204977 Ensembl
AllianceGenome	HGNC:9976

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000420995.6	hg38	chr13	49,997,019	50,014,331	17,313
ENST00000356017.8	hg38	chr13	49,997,037	50,013,180	16,144
ENST00000457662.2	hg38	chr13	49,997,059	50,013,168	16,110
ENST00000378182.4	hg38	chr13	49,997,042	50,018,467	21,426
ENST00000420995.6	hg19	chr13	50,571,155	50,588,467	17,313
ENST00000356017.8	hg19	chr13	50,571,173	50,587,316	16,144
ENST00000378182.4	hg19	chr13	50,571,178	50,592,603	21,426
ENST00000457662.2	hg19	chr13	50,571,195	50,587,304	16,110

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