MIAT myocardial infarction associated transcript

Information
Symbol
MIAT
Type
ncRNA
Description
myocardial infarction associated transcript
Entrez Gene ID
440823
Genome
hg19
Position
chr22:27,053,484-27,072,438
Genome
hg38
Position
chr22:26,657,520-26,676,475
MIM
611082 OMIM
HGNC
HGNC:33425 HGNC
Ensembl
ENSG00000225783 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 C22orf35
SYNONYM GOMAFU
SYNONYM LINC00066
SYNONYM NCRNA00066
SYNONYM RNCR2
SYNONYM lncRNA-MIAT
MIM 611082 OMIM
HGNC HGNC:33425 HGNC
Ensembl ENSG00000225783 Ensembl
AllianceGenome HGNC:33425
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000668051.1 hg38 chr22 26,646,411 26,666,225 19,815
ENST00000413665.6 hg38 chr22 26,657,458 26,666,220 8,763
ENST00000643270.1 hg38 chr22 26,646,452 26,669,655 23,204
ENST00000613780.4 hg38 chr22 26,657,520 26,676,475 18,956
ENST00000452429.5 hg38 chr22 26,657,284 26,666,023 8,740
ENST00000413665.6 hg19 chr22 27,053,422 27,062,184 8,763
ENST00000452429.5 hg19 chr22 27,053,248 27,061,987 8,740
ENST00000613780.4 hg19 chr22 27,053,484 27,072,438 18,955
ENST00000668051.1 hg19 chr22 27,042,375 27,062,189 19,815
ENST00000643270.1 hg19 chr22 27,042,416 27,065,618 23,203
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