MIR924HG MIR924 host gene

Information
Symbol
MIR924HG
Type
ncRNA
Description
MIR924 host gene
Entrez Gene ID
647946
Genome
hg19
Position
chr18:36,786,881-37,331,353
Genome
hg38
Position
chr18:39,206,917-39,751,389
HGNC
HGNC:44332 HGNC
Ensembl
ENSG00000267374 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
SYNONYM LINC00669
HGNC HGNC:44332 HGNC
Ensembl ENSG00000267374 Ensembl
AllianceGenome HGNC:44332
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000660099.1 hg38 chr18 39,207,023 39,800,272 593,250
ENST00000657401.1 hg38 chr18 39,781,349 39,800,316 18,968
ENST00000665416.1 hg38 chr18 39,207,258 39,800,298 593,041
ENST00000667009.1 hg38 chr18 39,206,919 39,751,372 544,454
ENST00000658956.1 hg38 chr18 39,648,848 39,800,322 151,475
ENST00000666611.1 hg38 chr18 39,206,918 39,800,294 593,377
ENST00000669399.1 hg38 chr18 39,206,917 39,751,389 544,473
ENST00000655721.1 hg38 chr18 39,207,122 39,535,523 328,402
ENST00000591469.1 hg38 chr18 39,207,627 39,340,638 133,012
ENST00000665844.1 hg38 chr18 39,206,927 39,752,060 545,134
ENST00000670943.1 hg38 chr18 39,275,638 39,751,938 476,301
ENST00000654966.1 hg38 chr18 39,348,579 39,800,309 451,731
ENST00000667816.1 hg38 chr18 39,206,917 39,751,960 545,044
ENST00000660099.1 hg19 chr18 36,786,987 37,380,236 593,250
ENST00000591469.1 hg19 chr18 36,787,591 36,920,602 133,012
ENST00000655721.1 hg19 chr18 36,787,086 37,115,487 328,402
ENST00000654966.1 hg19 chr18 36,928,543 37,380,273 451,731
ENST00000658956.1 hg19 chr18 37,228,812 37,380,286 151,475
ENST00000657401.1 hg19 chr18 37,361,313 37,380,280 18,968
ENST00000669399.1 hg19 chr18 36,786,881 37,331,353 544,473
ENST00000667009.1 hg19 chr18 36,786,883 37,331,336 544,454
ENST00000667816.1 hg19 chr18 36,786,881 37,331,924 545,044
ENST00000666611.1 hg19 chr18 36,786,882 37,380,258 593,377
ENST00000665844.1 hg19 chr18 36,786,891 37,332,024 545,134
ENST00000665416.1 hg19 chr18 36,787,222 37,380,262 593,041
ENST00000670943.1 hg19 chr18 36,855,602 37,331,902 476,301
Genome browser