MIR4770 microRNA 4770

Information
Symbol
MIR4770
Type
ncRNA
Description
microRNA 4770
Entrez Gene ID
100616373
Genome
hg19
Position
chrX:6,301,947-6,302,004
Genome
hg38
Position
chrX:6,383,906-6,383,963
HGNC
HGNC:41542 HGNC
Ensembl
ENSG00000265284 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 7 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:41542 HGNC
Ensembl ENSG00000265284 Ensembl
miRBase MI0017411
AllianceGenome HGNC:41542
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000579149.1 hg38 chrX 6,383,906 6,383,963 58
ENST00000579149.1 hg19 chrX 6,301,947 6,302,004 58
Genome browser