DHX37 DEAH-box helicase 37

Information
Symbol
DHX37
Type
protein-coding
Description
DEAH-box helicase 37
Entrez Gene ID
57647
Genome
hg19
Position
chr12:125,431,372-125,473,677
Genome
hg38
Position
chr12:124,946,826-124,989,131
MIM
617362 OMIM
HGNC
HGNC:17210 HGNC
Ensembl
ENSG00000150990 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 12
Likely pathogenic 0 22
Benign 0 126
Likely benign 0 288
Conflicting classifications of pathogenicity 0 18
Uncertain significance 0 402
Ranking
ClinVar
0
0
162
668
14
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 DDX37
SYNONYM Dhr1
SYNONYM NEDBAVC
SYNONYM SRXY11
MIM 617362 OMIM
HGNC HGNC:17210 HGNC
Ensembl ENSG00000150990 Ensembl
AllianceGenome HGNC:17210
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000308736.7 hg38 chr12 124,946,826 124,989,131 42,306
ENST00000308736.7 hg19 chr12 125,431,372 125,473,677 42,306
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