MIR4492 microRNA 4492

Information
Symbol
MIR4492
Type
ncRNA
Description
microRNA 4492
Entrez Gene ID
100616376
Genome
hg19
Position
chr11:118,781,417-118,781,496
Genome
hg38
Position
chr11:118,910,708-118,910,787
HGNC
HGNC:41563 HGNC
Ensembl
ENSG00000264211 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-4492
HGNC HGNC:41563 HGNC
Ensembl ENSG00000264211 Ensembl
miRBase MI0016854
AllianceGenome HGNC:41563
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000581627.1 hg38 chr11 118,910,708 118,910,787 80
ENST00000581627.1 hg19 chr11 118,781,417 118,781,496 80
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