MIR4785 microRNA 4785

Information
Symbol
MIR4785
Type
ncRNA
Description
microRNA 4785
Entrez Gene ID
100616364
Genome
hg38
Position
chr2:160,407,810-160,407,882
HGNC
HGNC:41889 HGNC
Ensembl
ENSG00000283734 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
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-4785
HGNC HGNC:41889 HGNC
Ensembl ENSG00000283734 Ensembl
miRBase MI0017430
AllianceGenome HGNC:41889
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000585005.1 hg38 chr2 160,407,810 160,407,882 73
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