APLNR apelin receptor

Information
Symbol
APLNR
Type
protein-coding
Description
apelin receptor
Entrez Gene ID
187
Genome
hg19
Position
chr11:57,001,065-57,004,724
Genome
hg38
Position
chr11:57,233,591-57,237,250
MIM
600052 OMIM
HGNC
HGNC:339 HGNC
Ensembl
ENSG00000134817 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 6
Uncertain significance 0 48
Ranking
ClinVar
0
0
0
56
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 :
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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 AGTRL1
SYNONYM APJ
SYNONYM APJR
SYNONYM HG11
MIM 600052 OMIM
HGNC HGNC:339 HGNC
Ensembl ENSG00000134817 Ensembl
AllianceGenome HGNC:339
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000606794.2 hg38 chr11 57,233,591 57,237,250 3,660
ENST00000606794.2 hg19 chr11 57,001,065 57,004,724 3,660
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