MIR4789 microRNA 4789

Information
Symbol
MIR4789
Type
ncRNA
Description
microRNA 4789
Entrez Gene ID
100616395
Genome
hg19
Position
chr3:175,087,329-175,087,410
Genome
hg38
Position
chr3:175,369,540-175,369,621
HGNC
HGNC:41719 HGNC
Ensembl
ENSG00000264974 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
HGNC HGNC:41719 HGNC
Ensembl ENSG00000264974 Ensembl
miRBase MI0017436
AllianceGenome HGNC:41719
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000577469.1 hg38 chr3 175,369,540 175,369,621 82
ENST00000577469.1 hg19 chr3 175,087,329 175,087,410 82
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