MIR4769 microRNA 4769

Information
Symbol
MIR4769
Type
ncRNA
Description
microRNA 4769
Entrez Gene ID
100616147
Genome
hg19
Position
chrX:47,446,828-47,446,904
Genome
hg38
Position
chrX:47,587,429-47,587,505
HGNC
HGNC:41694 HGNC
Ensembl
ENSG00000263858 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 6 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:41694 HGNC
Ensembl ENSG00000263858 Ensembl
miRBase MI0017410
AllianceGenome HGNC:41694
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000584126.1 hg38 chrX 47,587,429 47,587,505 77
ENST00000584126.1 hg19 chrX 47,446,828 47,446,904 77
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