ENST00000651466.1 PELATON

Information
Transcript ID
ENST00000651466.1
Genome
hg38
Position
chr20:50,259,019-50,278,421
Strand
+
CDS length
0
Amino acid length
0
Gene symbol
PELATON
Gene type
ncRNA
Gene description
plaque enriched lncRNA in atherosclerotic and inflammatory bowel macrophage regulation
Gene Entrez Gene ID
100506115
Variants

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MGeND data only
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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
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MGeND data only
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Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
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MGeND data only
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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
Exon
Exon number Start Stop
1 50,259,019 50,259,557
2 50,264,202 50,264,323
3 50,275,646 50,275,735
4 50,276,057 50,276,390
5 50,277,491 50,277,980
6 50,278,177 50,278,421
Other genome
Genome Chromosome Start End Links
hg19 chr20 48,875,556 48,894,958 Link
CDS sequence
Amino sequence