MIR509-1 microRNA 509-1

Information
Symbol
MIR509-1
Type
ncRNA
Description
microRNA 509-1
Entrez Gene ID
574514
Genome
hg19
Position
chrX:146,342,050-146,342,143
Genome
hg38
Position
chrX:147,260,532-147,260,625
MIM
300875 OMIM
HGNC
HGNC:32146 HGNC
Ensembl
ENSG00000208000 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 6 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 MIRN509
SYNONYM MIRN509-1
SYNONYM hsa-mir-509
SYNONYM mir-509-1
MIM 300875 OMIM
HGNC HGNC:32146 HGNC
Ensembl ENSG00000208000 Ensembl
miRBase MI0003196
AllianceGenome HGNC:32146
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000385265.1 hg38 chrX 147,260,532 147,260,625 94
ENST00000385265.1 hg19 chrX 146,342,050 146,342,143 94
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