MIR507 microRNA 507

Information
Symbol
MIR507
Type
ncRNA
Description
microRNA 507
Entrez Gene ID
574512
Genome
hg19
Position
chrX:146,312,502-146,312,595
Genome
hg38
Position
chrX:147,230,984-147,231,077
HGNC
HGNC:32144 HGNC
Ensembl
ENSG00000207969 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 MIRN507
SYNONYM hsa-mir-507
SYNONYM mir-507
HGNC HGNC:32144 HGNC
Ensembl ENSG00000207969 Ensembl
miRBase MI0003194
AllianceGenome HGNC:32144
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000385234.1 hg38 chrX 147,230,984 147,231,077 94
ENST00000385234.1 hg19 chrX 146,312,502 146,312,595 94
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