MIR4759 microRNA 4759

Information
Symbol
MIR4759
Type
ncRNA
Description
microRNA 4759
Entrez Gene ID
100616243
Genome
hg19
Position
chr21:28,326,280-28,326,362
Genome
hg38
Position
chr21:26,953,961-26,954,043
HGNC
HGNC:41575 HGNC
Ensembl
ENSG00000266133 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:41575 HGNC
Ensembl ENSG00000266133 Ensembl
miRBase MI0017400
AllianceGenome HGNC:41575
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000584048.1 hg38 chr21 26,953,961 26,954,043 83
ENST00000584048.1 hg19 chr21 28,326,280 28,326,362 83
Genome browser