P2RY12 purinergic receptor P2Y12

Information
Symbol
P2RY12
Type
protein-coding
Description
purinergic receptor P2Y12
Entrez Gene ID
64805
Genome
hg19
Position
chr3:151,054,631-151,102,541
Genome
hg38
Position
chr3:151,336,843-151,384,753
MIM
600515 OMIM
HGNC
HGNC:18124 HGNC
Ensembl
ENSG00000169313 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 16
Likely pathogenic 0 16
Benign 0 32
Likely benign 0 76
Conflicting classifications of pathogenicity 0 4
Uncertain significance 0 200
Ranking
ClinVar
0
0
44
282
10
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 :
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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 ADPG-R
SYNONYM BDPLT8
SYNONYM HORK3
SYNONYM P2T(AC)
SYNONYM P2Y(12)R
SYNONYM P2Y(AC)
SYNONYM P2Y(ADP)
SYNONYM P2Y(cyc)
SYNONYM P2Y12
SYNONYM SP1999
MIM 600515 OMIM
HGNC HGNC:18124 HGNC
Ensembl ENSG00000169313 Ensembl
AllianceGenome HGNC:18124
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000302632.4 hg38 chr3 151,336,843 151,384,753 47,911
ENST00000302632.4 hg19 chr3 151,054,631 151,102,541 47,911
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