MIR1178 microRNA 1178

Information
Symbol
MIR1178
Type
ncRNA
Description
microRNA 1178
Entrez Gene ID
100302274
Genome
hg38
Position
chr12:119,713,634-119,713,724
HGNC
HGNC:35259 HGNC
Ensembl
ENSG00000283768 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
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
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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 :
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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 MIRN1178
SYNONYM hsa-mir-1178
HGNC HGNC:35259 HGNC
Ensembl ENSG00000283768 Ensembl
miRBase MI0006271
AllianceGenome HGNC:35259
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000408396.1 hg38 chr12 119,713,634 119,713,724 91
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