MIR4667 microRNA 4667

Information
Symbol
MIR4667
Type
ncRNA
Description
microRNA 4667
Entrez Gene ID
100616214
Genome
hg19
Position
chr9:35,608,091-35,608,156
Genome
hg38
Position
chr9:35,608,094-35,608,159
HGNC
HGNC:41723 HGNC
Ensembl
ENSG00000263892 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-4667
HGNC HGNC:41723 HGNC
Ensembl ENSG00000263892 Ensembl
miRBase MI0017297
AllianceGenome HGNC:41723
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000578933.3 hg38 chr9 35,608,094 35,608,159 66
ENST00000578933.1 hg19 chr9 35,608,091 35,608,156 66
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