PPAN-P2RY11 PPAN-P2RY11 readthrough

Information
Symbol
PPAN-P2RY11
Type
protein-coding
Description
PPAN-P2RY11 readthrough
Entrez Gene ID
692312
Genome
hg19
Position
chr19:10,217,071-10,225,414
Genome
hg38
Position
chr19:10,106,395-10,114,738
HGNC
HGNC:33526 HGNC
Ensembl
ENSG00000243207 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 22
Likely benign 0 50
association 0 4
Uncertain significance 0 18
Ranking
ClinVar
0
0
8
78
4
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
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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 :
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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
TypeID
SYNONYM BXDC3
SYNONYM P2RY11
SYNONYM P2Y11
SYNONYM PPAN
SYNONYM SSF1
SYNONYM Ssf-1
HGNC HGNC:33526 HGNC
Ensembl ENSG00000243207 Ensembl
AllianceGenome HGNC:33526
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000428358.5 hg38 chr19 10,106,223 10,114,780 8,558
ENST00000393796.4 hg38 chr19 10,106,395 10,114,738 8,344
ENST00000428358.5 hg19 chr19 10,216,899 10,225,456 8,558
ENST00000393796.4 hg19 chr19 10,217,071 10,225,414 8,344
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