MIR4767 microRNA 4767

Information
Symbol
MIR4767
Type
ncRNA
Description
microRNA 4767
Entrez Gene ID
100616467
Genome
hg19
Position
chrX:7,065,901-7,065,978
Genome
hg38
Position
chrX:7,147,860-7,147,937
HGNC
HGNC:41548 HGNC
Ensembl
ENSG00000264268 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 10 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
SYNONYM mir-4767
HGNC HGNC:41548 HGNC
Ensembl ENSG00000264268 Ensembl
miRBase MI0017408
AllianceGenome HGNC:41548
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000582827.1 hg38 chrX 7,147,860 7,147,937 78
ENST00000582827.1 hg19 chrX 7,065,901 7,065,978 78
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