MIR5011 microRNA 5011

Information
Symbol
MIR5011
Type
ncRNA
Description
microRNA 5011
Entrez Gene ID
100847002
Genome
hg19
Position
chr18:64,748,821-64,748,923
Genome
hg38
Position
chr18:67,081,584-67,081,686
HGNC
HGNC:43496 HGNC
Ensembl
ENSG00000263354 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:43496 HGNC
Ensembl ENSG00000263354 Ensembl
miRBase MI0017879
AllianceGenome HGNC:43496
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000578054.1 hg38 chr18 67,081,584 67,081,686 103
ENST00000578054.1 hg19 chr18 64,748,821 64,748,923 103
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