MIR4753 microRNA 4753

Information
Symbol
MIR4753
Type
ncRNA
Description
microRNA 4753
Entrez Gene ID
100616224
Genome
hg19
Position
chr1:235,353,349-235,353,431
Genome
hg38
Position
chr1:235,190,034-235,190,116
HGNC
HGNC:41527 HGNC
Ensembl
ENSG00000263439 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-4753
HGNC HGNC:41527 HGNC
Ensembl ENSG00000263439 Ensembl
miRBase MI0017392
AllianceGenome HGNC:41527
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000585119.1 hg38 chr1 235,190,034 235,190,116 83
ENST00000585119.1 hg19 chr1 235,353,349 235,353,431 83
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