MIR5007 microRNA 5007

Information
Symbol
MIR5007
Type
ncRNA
Description
microRNA 5007
Entrez Gene ID
100846996
Genome
hg19
Position
chr13:55,748,589-55,748,683
Genome
hg38
Position
chr13:55,174,454-55,174,548
HGNC
HGNC:43468 HGNC
Ensembl
ENSG00000264387 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
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
HGNC HGNC:43468 HGNC
Ensembl ENSG00000264387 Ensembl
miRBase MI0017874
AllianceGenome HGNC:43468
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000583098.1 hg38 chr13 55,174,454 55,174,548 95
ENST00000583098.1 hg19 chr13 55,748,589 55,748,683 95
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