MIR4500HG MIR4500 host gene

Information
Symbol
MIR4500HG
Type
ncRNA
Description
MIR4500 host gene
Entrez Gene ID
642345
Genome
hg19
Position
chr13:88,264,772-88,323,881
Genome
hg38
Position
chr13:87,612,517-87,671,626
HGNC
HGNC:42773 HGNC
Ensembl
ENSG00000228824 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
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 :
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
HGNC HGNC:42773 HGNC
Ensembl ENSG00000228824 Ensembl
AllianceGenome HGNC:42773
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000668695.1 hg38 chr13 87,583,783 87,671,629 87,847
ENST00000658270.1 hg38 chr13 87,609,602 87,671,450 61,849
ENST00000436290.2 hg38 chr13 87,443,987 87,670,963 226,977
ENST00000658012.1 hg38 chr13 87,583,766 87,671,297 87,532
ENST00000656584.1 hg38 chr13 87,612,531 87,671,613 59,083
ENST00000685035.1 hg38 chr13 87,614,650 87,671,101 56,452
ENST00000660424.1 hg38 chr13 87,612,517 87,671,626 59,110
ENST00000441617.7 hg38 chr13 87,583,722 87,671,324 87,603
ENST00000436290.2 hg19 chr13 88,096,242 88,323,218 226,977
ENST00000441617.7 hg19 chr13 88,235,977 88,323,579 87,603
ENST00000656584.1 hg19 chr13 88,264,786 88,323,868 59,083
ENST00000658012.1 hg19 chr13 88,236,021 88,323,552 87,532
ENST00000658270.1 hg19 chr13 88,261,857 88,323,705 61,849
ENST00000660424.1 hg19 chr13 88,264,772 88,323,881 59,110
ENST00000668695.1 hg19 chr13 88,236,038 88,323,884 87,847
ENST00000685035.1 hg19 chr13 88,266,905 88,323,356 56,452
Genome browser