MIR569 microRNA 569

Information
Symbol
MIR569
Type
ncRNA
Description
microRNA 569
Entrez Gene ID
693154
Genome
hg19
Position
chr3:170,824,453-170,824,548
Genome
hg38
Position
chr3:171,106,664-171,106,759
HGNC
HGNC:32825 HGNC
Ensembl
ENSG00000207963 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 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
SYNONYM MIRN569
SYNONYM hsa-mir-569
HGNC HGNC:32825 HGNC
Ensembl ENSG00000207963 Ensembl
miRBase MI0003576
AllianceGenome HGNC:32825
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000385228.1 hg38 chr3 171,106,664 171,106,759 96
ENST00000385228.1 hg19 chr3 170,824,453 170,824,548 96
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