CISD2 CDGSH iron sulfur domain 2

Information
Symbol
CISD2
Type
protein-coding
Description
CDGSH iron sulfur domain 2
Entrez Gene ID
493856
Genome
hg19
Position
chr4:103,790,149-103,813,964
Genome
hg38
Position
chr4:102,868,992-102,892,807
MIM
611507 OMIM
HGNC
HGNC:24212 HGNC
Ensembl
ENSG00000145354 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 4
Benign 0 8
Likely benign 0 64
Conflicting classifications of pathogenicity 0 4
not provided 35 0
Uncertain significance 0 38
Ranking
ClinVar
0
0
18
84
6
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
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
Entry Origin Type Annotation Entry Origin Annotation
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
Entry Origin Type Annotation
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
Entry Origin Type Annotation
TypeID
SYNONYM ERIS
SYNONYM Miner1
SYNONYM NAF-1
SYNONYM WFS2
SYNONYM ZCD2
MIM 611507 OMIM
HGNC HGNC:24212 HGNC
Ensembl ENSG00000145354 Ensembl
AllianceGenome HGNC:24212
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000273986.10 hg38 chr4 102,868,992 102,892,807 23,816
ENST00000503643.1 hg38 chr4 102,869,336 102,887,756 18,421
ENST00000273986.10 hg19 chr4 103,790,149 103,813,964 23,816
ENST00000503643.1 hg19 chr4 103,790,493 103,808,913 18,421
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