MIR4765 microRNA 4765

Information
Symbol
MIR4765
Type
ncRNA
Description
microRNA 4765
Entrez Gene ID
100616219
Genome
hg19
Position
chr2:32,860,322-32,860,398
Genome
hg38
Position
chr2:32,635,255-32,635,331
HGNC
HGNC:41791 HGNC
Ensembl
ENSG00000265057 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:41791 HGNC
Ensembl ENSG00000265057 Ensembl
miRBase MI0017406
AllianceGenome HGNC:41791
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000585007.1 hg38 chr2 32,635,255 32,635,331 77
ENST00000585007.1 hg19 chr2 32,860,322 32,860,398 77
Genome browser