OBI1-AS1 OBI1 antisense RNA 1

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: OBI1-AS1
Type: ncRNA
Description: OBI1 antisense RNA 1
Entrez Gene ID: 100874222
Genome: hg19
Position: chr13:78,493,824-79,158,297
Genome: hg38
Position: chr13:77,919,689-78,584,162
HGNC: HGNC:42700 HGNC
Ensembl: ENSG00000234377 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Pathogenic	2	0

Ranking

	ClinVar
	0
	0
	0
	0
	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

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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	POU4F1-AS1
SYNONYM	RNF219-AS1
HGNC	HGNC:42700 HGNC
Ensembl	ENSG00000234377 Ensembl
AllianceGenome	HGNC:42700

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000607862.5	hg38	chr13	77,919,689	78,584,162	664,474
ENST00000607860.5	hg38	chr13	78,054,868	78,605,378	550,511
ENST00000606429.5	hg38	chr13	78,054,855	78,617,325	562,471
ENST00000444769.7	hg38	chr13	78,055,023	78,607,002	551,980
ENST00000605996.5	hg38	chr13	78,054,845	78,578,714	523,870
ENST00000607862.5	hg19	chr13	78,493,824	79,158,297	664,474
ENST00000605996.5	hg19	chr13	78,628,980	79,152,849	523,870
ENST00000606429.5	hg19	chr13	78,628,990	79,191,460	562,471
ENST00000607860.5	hg19	chr13	78,629,003	79,179,513	550,511
ENST00000444769.7	hg19	chr13	78,629,158	79,181,137	551,980

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