MIR6089 microRNA 6089

Information
Symbol
MIR6089
Type
ncRNA
Description
microRNA 6089
Entrez Gene ID
102464837
Genome
hg38
Position
chrY:2,609,191-2,609,254
Genome
hg38
Position
chrX:2,609,191-2,609,254
HGNC
HGNC:50179 HGNC
Ensembl
ENSG00000277120 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 8 0
Ranking
ClinVar
0
0
0
0
0
Frequency
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 MIR6089-1
SYNONYM MIR6089-2
SYNONYM hsa-mir-6089-1
SYNONYM hsa-mir-6089-2
HGNC HGNC:50179 HGNC
Ensembl ENSG00000277120 Ensembl
Ensembl ENSG00000292346 Ensembl
miRBase MI0020366
AllianceGenome HGNC:50179
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000711167.1 hg38 chrY 2,609,191 2,609,254 64
ENST00000616698.5 hg38 chrX 2,609,191 2,609,254 64
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