MIR502 microRNA 502

Information
Symbol
MIR502
Type
ncRNA
Description
microRNA 502
Entrez Gene ID
574504
Genome
hg19
Position
chrX:49,779,206-49,779,291
Genome
hg38
Position
chrX:50,014,598-50,014,683
MIM
300893 OMIM
HGNC
HGNC:32136 HGNC
Ensembl
ENSG00000272080 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 MIRN502
SYNONYM hsa-mir-502
SYNONYM mir-502
MIM 300893 OMIM
HGNC HGNC:32136 HGNC
Ensembl ENSG00000272080 Ensembl
miRBase MI0003186
AllianceGenome HGNC:32136
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000606349.1 hg38 chrX 50,014,598 50,014,683 86
ENST00000606349.1 hg19 chrX 49,779,206 49,779,291 86
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