MIR4768 microRNA 4768

Information
Symbol
MIR4768
Type
ncRNA
Description
microRNA 4768
Entrez Gene ID
100616249
Genome
hg19
Position
chrX:17,444,004-17,444,077
Genome
hg38
Position
chrX:17,425,881-17,425,954
HGNC
HGNC:41592 HGNC
Ensembl
ENSG00000265465 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:41592 HGNC
Ensembl ENSG00000265465 Ensembl
miRBase MI0017409
AllianceGenome HGNC:41592
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000585270.1 hg38 chrX 17,425,881 17,425,954 74
ENST00000585270.1 hg19 chrX 17,444,004 17,444,077 74
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