GPR89A G protein-coupled receptor 89A

Information
Symbol
GPR89A
Type
protein-coding
Description
G protein-coupled receptor 89A
Entrez Gene ID
653519
Genome
hg19
Position
chr1:145,764,409-145,827,075
Genome
hg38
Position
chr1:145,607,988-145,670,650
MIM
612821 OMIM
HGNC
HGNC:31984 HGNC
Ensembl
ENSG00000117262 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 2 0
Uncertain significance 0 20
Ranking
ClinVar
0
0
0
20
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
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 GPHR
SYNONYM GPR89
SYNONYM GPR89B
SYNONYM SH120
SYNONYM UNQ192
MIM 612821 OMIM
HGNC HGNC:31984 HGNC
Ensembl ENSG00000117262 Ensembl
AllianceGenome HGNC:31984
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000534502.5 hg38 chr1 145,608,048 145,670,184 62,137
ENST00000462900.2 hg38 chr1 145,608,613 145,670,178 61,566
ENST00000313835.14 hg38 chr1 145,607,988 145,670,650 62,663
ENST00000313835.14 hg19 chr1 145,764,409 145,827,075 62,667
ENST00000534502.5 hg19 chr1 145,764,875 145,827,015 62,141
ENST00000462900.2 hg19 chr1 145,764,881 145,826,450 61,570
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