DHX9 DExH-box helicase 9

Information
Symbol
DHX9
Type
protein-coding
Description
DExH-box helicase 9
Entrez Gene ID
1660
Genome
hg19
Position
chr1:182,808,482-182,857,117
Genome
hg38
Position
chr1:182,839,347-182,887,982
MIM
603115 OMIM
HGNC
HGNC:2750 HGNC
Ensembl
ENSG00000135829 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 6
Benign 0 8
Uncertain significance 0 60
Ranking
ClinVar
0
0
0
70
4
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
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 DDX9
SYNONYM LKP
SYNONYM NDH2
SYNONYM NDHII
SYNONYM RHA
MIM 603115 OMIM
HGNC HGNC:2750 HGNC
Ensembl ENSG00000135829 Ensembl
AllianceGenome HGNC:2750
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000367549.4 hg38 chr1 182,839,347 182,887,982 48,636
ENST00000367549.4 hg19 chr1 182,808,482 182,857,117 48,636
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