DDX25 DEAD-box helicase 25

Information
Symbol
DDX25
Type
protein-coding
Description
DEAD-box helicase 25
Entrez Gene ID
29118
Genome
hg19
Position
chr11:125,774,403-125,798,738
Genome
hg38
Position
chr11:125,904,508-125,928,843
MIM
607663 OMIM
HGNC
HGNC:18698 HGNC
Ensembl
ENSG00000109832 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Benign 0 50
Likely benign 0 2
Uncertain significance 0 60
Ranking
ClinVar
0
0
0
112
2
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 :
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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 GRTH
MIM 607663 OMIM
HGNC HGNC:18698 HGNC
Ensembl ENSG00000109832 Ensembl
AllianceGenome HGNC:18698
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000525943.1 hg38 chr11 125,903,376 125,923,083 19,708
ENST00000263576.11 hg38 chr11 125,904,508 125,928,843 24,336
ENST00000525943.1 hg19 chr11 125,773,271 125,792,978 19,708
ENST00000263576.11 hg19 chr11 125,774,403 125,798,738 24,336
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