MIR448 microRNA 448

Information
Symbol
MIR448
Type
ncRNA
Description
microRNA 448
Entrez Gene ID
554212
Genome
hg19
Position
chrX:114,058,017-114,058,127
Genome
hg38
Position
chrX:114,823,454-114,823,564
MIM
300686 OMIM
HGNC
HGNC:26069 HGNC
Ensembl
ENSG00000199001 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 7 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 MIRN448
SYNONYM hsa-mir-448
SYNONYM miRNA448
MIM 300686 OMIM
HGNC HGNC:26069 HGNC
Ensembl ENSG00000199001 Ensembl
miRBase MI0001637
AllianceGenome HGNC:26069
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000362131.1 hg38 chrX 114,823,454 114,823,564 111
ENST00000362131.1 hg19 chrX 114,058,017 114,058,127 111
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