P2RX5-TAX1BP3 P2RX5-TAX1BP3 readthrough (NMD candidate)

Information
Symbol
P2RX5-TAX1BP3
Type
ncRNA
Description
P2RX5-TAX1BP3 readthrough (NMD candidate)
Entrez Gene ID
100533970
Genome
hg19
Position
chr17:3,566,357-3,599,488
Genome
hg38
Position
chr17:3,663,063-3,696,194
HGNC
HGNC:49191 HGNC
Ensembl
ENSG00000257950 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 16
Likely benign 0 8
Conflicting classifications of pathogenicity 0 4
Uncertain significance 0 114
Ranking
ClinVar
0
0
6
128
2
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 :
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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
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 P2RX5
SYNONYM P2X5
HGNC HGNC:49191 HGNC
Ensembl ENSG00000257950 Ensembl
AllianceGenome HGNC:49191
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000550383.1 hg38 chr17 3,663,063 3,696,194 33,132
ENST00000550383.1 hg19 chr17 3,566,357 3,599,488 33,132
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