DDX17 DEAD-box helicase 17

Information
Symbol
DDX17
Type
protein-coding
Description
DEAD-box helicase 17
Entrez Gene ID
10521
Genome
hg19
Position
chr22:38,879,445-38,902,342
Genome
hg38
Position
chr22:38,483,440-38,506,337
MIM
608469 OMIM
HGNC
HGNC:2740 HGNC
Ensembl
ENSG00000100201 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
not provided 0 2
Ranking
ClinVar
0
0
0
2
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
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 P72
SYNONYM RH70
MIM 608469 OMIM
HGNC HGNC:2740 HGNC
Ensembl ENSG00000100201 Ensembl
AllianceGenome HGNC:2740
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000403230.3 hg38 chr22 38,483,438 38,506,311 22,874
ENST00000396821.8 hg38 chr22 38,483,440 38,506,337 22,898
ENST00000403230.3 hg19 chr22 38,879,443 38,902,316 22,874
ENST00000396821.8 hg19 chr22 38,879,445 38,902,342 22,898
Genome browser