CISD3 CDGSH iron sulfur domain 3

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Variants
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Information

Symbol: CISD3
Type: protein-coding
Description: CDGSH iron sulfur domain 3
Entrez Gene ID: 284106
Genome: hg19
Position: chr17:36,886,594-36,891,858
Genome: hg38
Position: chr17:38,730,341-38,735,605
MIM: 611933 OMIM
HGNC: HGNC:27578 HGNC
Ensembl: ENSG00000277972 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	14
Likely benign	0	44
Conflicting classifications of pathogenicity	0	4
Uncertain significance	0	102

Ranking

	ClinVar
	0
	0
	22
	138
	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

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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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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	MiNT
SYNONYM	Miner2
MIM	611933 OMIM
HGNC	HGNC:27578 HGNC
Ensembl	ENSG00000277972 Ensembl
AllianceGenome	HGNC:27578

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000613478.2	hg38	chr17	38,730,341	38,735,605	5,265
ENST00000613478.2	hg19	chr17	36,886,594	36,891,858	5,265

Key	Value
strand	+
start	36,886,509
Gene Symbol	CISD3
Entrez GeneId	284,106
Chr Band	17q12
end	36,891,857
chr	chr17

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