NEAT1 nuclear paraspeckle assembly transcript 1

Information
Symbol
NEAT1
Type
ncRNA
Description
nuclear paraspeckle assembly transcript 1
Entrez Gene ID
283131
Genome
hg19
Position
chr11:65,190,269-65,213,011
Genome
hg38
Position
chr11:65,422,798-65,445,540
MIM
612769 OMIM
HGNC
HGNC:30815 HGNC
Ensembl
ENSG00000245532 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 LINC00084
SYNONYM NCRNA00084
SYNONYM TP53LC15
SYNONYM TncRNA
SYNONYM VINC
MIM 612769 OMIM
HGNC HGNC:30815 HGNC
Ensembl ENSG00000245532 Ensembl
AllianceGenome HGNC:30815
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000601801.3 hg38 chr11 65,422,800 65,426,405 3,606
ENST00000499732.3 hg38 chr11 65,422,774 65,426,457 3,684
ENST00000501122.2 hg38 chr11 65,422,798 65,445,540 22,743
ENST00000645023.1 hg38 chr11 65,423,125 65,426,499 3,375
ENST00000616315.2 hg38 chr11 65,425,551 65,426,385 835
ENST00000612303.2 hg38 chr11 65,422,804 65,424,404 1,601
ENST00000642367.1 hg38 chr11 65,423,539 65,424,967 1,429
ENST00000646243.1 hg38 chr11 65,423,096 65,426,513 3,418
ENST00000499732.3 hg19 chr11 65,190,245 65,193,928 3,684
ENST00000501122.2 hg19 chr11 65,190,269 65,213,011 22,743
ENST00000601801.3 hg19 chr11 65,190,271 65,193,876 3,606
ENST00000612303.2 hg19 chr11 65,190,275 65,191,875 1,601
ENST00000646243.1 hg19 chr11 65,190,567 65,193,984 3,418
ENST00000645023.1 hg19 chr11 65,190,596 65,193,970 3,375
ENST00000642367.1 hg19 chr11 65,191,010 65,192,438 1,429
ENST00000616315.2 hg19 chr11 65,193,022 65,193,856 835
Genome browser