MIR4665 microRNA 4665

Information
Symbol
MIR4665
Type
ncRNA
Description
microRNA 4665
Entrez Gene ID
100616288
Genome
hg19
Position
chr9:6,007,826-6,007,904
Genome
hg38
Position
chr9:6,007,826-6,007,904
HGNC
HGNC:41696 HGNC
Ensembl
ENSG00000263575 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
SYNONYM mir-4665
HGNC HGNC:41696 HGNC
Ensembl ENSG00000263575 Ensembl
miRBase MI0017295
AllianceGenome HGNC:41696
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000581132.1 hg38 chr9 6,007,826 6,007,904 79
ENST00000581132.1 hg19 chr9 6,007,826 6,007,904 79
Genome browser