MIR4772 microRNA 4772

Information
Symbol
MIR4772
Type
ncRNA
Description
microRNA 4772
Entrez Gene ID
100616157
Genome
hg19
Position
chr2:103,048,749-103,048,826
Genome
hg38
Position
chr2:102,432,289-102,432,366
HGNC
HGNC:41741 HGNC
Ensembl
ENSG00000264764 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-4772
HGNC HGNC:41741 HGNC
Ensembl ENSG00000264764 Ensembl
miRBase MI0017414
AllianceGenome HGNC:41741
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000581495.1 hg38 chr2 102,432,289 102,432,366 78
ENST00000581495.1 hg19 chr2 103,048,749 103,048,826 78
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