TP53TG1 TP53 target 1

Information
Symbol
TP53TG1
Type
ncRNA
Description
TP53 target 1
Entrez Gene ID
11257
Genome
hg19
Position
chr7:86,952,259-86,974,867
Genome
hg38
Position
chr7:87,322,943-87,345,551
MIM
616403 OMIM
HGNC
HGNC:17026 HGNC
Ensembl
ENSG00000182165 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 LINC00096
SYNONYM NCRNA00096
SYNONYM P53TG1
SYNONYM P53TG1-D
SYNONYM TP53AP1
SYNONYM TP53LC12
MIM 616403 OMIM
HGNC HGNC:17026 HGNC
Ensembl ENSG00000182165 Ensembl
AllianceGenome HGNC:17026
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000687819.1 hg38 chr7 87,325,347 87,345,507 20,161
ENST00000661943.3 hg38 chr7 87,322,943 87,345,551 22,609
ENST00000701419.1 hg38 chr7 87,325,352 87,345,457 20,106
ENST00000661943.3 hg19 chr7 86,952,259 86,974,867 22,609
ENST00000687819.1 hg19 chr7 86,954,663 86,974,823 20,161
ENST00000701419.1 hg19 chr7 86,954,668 86,974,773 20,106
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