MIR4742 microRNA 4742

Information
Symbol
MIR4742
Type
ncRNA
Description
microRNA 4742
Entrez Gene ID
100616468
Genome
hg19
Position
chr1:224,585,929-224,586,013
Genome
hg38
Position
chr1:224,398,227-224,398,311
HGNC
HGNC:41565 HGNC
Ensembl
ENSG00000266618 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-4742
HGNC HGNC:41565 HGNC
Ensembl ENSG00000266618 Ensembl
miRBase MI0017380
AllianceGenome HGNC:41565
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000581069.1 hg38 chr1 224,398,227 224,398,311 85
ENST00000581069.1 hg19 chr1 224,585,929 224,586,013 85
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