ENST00000663009.2 PELATON

Information
Transcript ID
ENST00000663009.2
Genome
hg38
Position
chr20:50,276,289-50,283,250
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

Display target variant


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
Exon
Exon number Start Stop
1 50,276,289 50,276,390
2 50,277,491 50,277,613
3 50,278,177 50,281,865
4 50,282,553 50,283,250
Other genome
Genome Chromosome Start End Links
hg19 chr20 48,892,826 48,899,787 Link
CDS sequence
Amino sequence