TXLNG taxilin gamma

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: TXLNG
Type: protein-coding
Description: taxilin gamma
Entrez Gene ID: 55787
Genome: hg19
Position: chrX:16,804,589-16,862,642
Genome: hg38
Position: chrX:16,786,466-16,844,519
MIM: 300677 OMIM
HGNC: HGNC:18578 HGNC
Ensembl: ENSG00000086712 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	2
Likely benign	0	6
not provided	7	0
Uncertain significance	0	40

Ranking

	ClinVar
	0
	0
	0
	48
	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

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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	CXorf15
SYNONYM	ELRG
SYNONYM	FIAT
SYNONYM	LSR5
SYNONYM	TXLNGX
MIM	300677 OMIM
HGNC	HGNC:18578 HGNC
Ensembl	ENSG00000086712 Ensembl
AllianceGenome	HGNC:18578

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000380122.10	hg38	chrX	16,786,466	16,844,519	58,054
ENST00000398155.4	hg38	chrX	16,786,432	16,844,517	58,086
ENST00000398155.4	hg19	chrX	16,804,555	16,862,640	58,086
ENST00000380122.10	hg19	chrX	16,804,589	16,862,642	58,054

Key	Value
strand	+
start	16,804,554
Gene Symbol	TXLNG
Entrez GeneId	55,787
Chr Band	Xp22.2
end	16,862,641
chr	chrX

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