DAOA D-amino acid oxidase activator

Go to:

Information
Clinical Significance
Ranking
Frequency
Disease area statistics
Locus Zoom
Variants
Genome browser

Information

Symbol: DAOA
Type: protein-coding
Description: D-amino acid oxidase activator
Entrez Gene ID: 267012
Genome: hg19
Position: chr13:106,118,394-106,143,383
Genome: hg38
Position: chr13:105,466,045-105,491,034
MIM: 607408 OMIM
HGNC: HGNC:21191 HGNC
Ensembl: ENSG00000182346 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	6
Likely benign	0	6
not provided	0	10
Uncertain significance	0	8

Ranking

	ClinVar
	0
	0
	0
	20
	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
Category	:
Search word	:
Filtering	:

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	:
Search word	:
Filtering	:

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	LG72
SYNONYM	SG72
MIM	607408 OMIM
HGNC	HGNC:21191 HGNC
Ensembl	ENSG00000182346 Ensembl
AllianceGenome	HGNC:21191

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000618629.1	hg38	chr13	105,466,289	105,490,987	24,699
ENST00000329625.9	hg38	chr13	105,466,270	105,490,987	24,718
ENST00000595812.2	hg38	chr13	105,466,270	105,490,987	24,718
ENST00000375936.9	hg38	chr13	105,466,045	105,491,034	24,990
ENST00000375936.9	hg19	chr13	106,118,394	106,143,383	24,990
ENST00000329625.9	hg19	chr13	106,118,619	106,143,336	24,718
ENST00000595812.2	hg19	chr13	106,118,619	106,143,336	24,718
ENST00000618629.1	hg19	chr13	106,118,638	106,143,336	24,699

Genome browser