MIR4760 microRNA 4760

Information
Symbol
MIR4760
Type
ncRNA
Description
microRNA 4760
Entrez Gene ID
100616148
Genome
hg19
Position
chr21:41,584,279-41,584,358
Genome
hg38
Position
chr21:40,212,352-40,212,431
HGNC
HGNC:41698 HGNC
Ensembl
ENSG00000263973 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 1 0
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
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:41698 HGNC
Ensembl ENSG00000263973 Ensembl
miRBase MI0017401
AllianceGenome HGNC:41698
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000585040.1 hg38 chr21 40,212,352 40,212,431 80
ENST00000585040.1 hg19 chr21 41,584,279 41,584,358 80
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