MIR767 microRNA 767

Information
Symbol
MIR767
Type
ncRNA
Description
microRNA 767
Entrez Gene ID
768215
Genome
hg19
Position
chrX:151,561,893-151,562,001
Genome
hg38
Position
chrX:152,393,421-152,393,529
HGNC
HGNC:33136 HGNC
Ensembl
ENSG00000211583 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 MIRN767
SYNONYM hsa-mir-767
SYNONYM mir-767
HGNC HGNC:33136 HGNC
Ensembl ENSG00000211583 Ensembl
miRBase MI0003763
AllianceGenome HGNC:33136
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000390228.3 hg38 chrX 152,393,421 152,393,529 109
ENST00000390228.1 hg19 chrX 151,561,893 151,562,001 109
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