GPR137 G protein-coupled receptor 137

Information
Symbol
GPR137
Type
protein-coding
Description
G protein-coupled receptor 137
Entrez Gene ID
56834
Genome
hg19
Position
chr11:64,051,811-64,056,876
Genome
hg38
Position
chr11:64,284,339-64,289,404
HGNC
HGNC:24300 HGNC
Ensembl
ENSG00000173264 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
32
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
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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 :
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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 :
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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 C11orf4
SYNONYM GPR137A
SYNONYM TM7SF1L1
HGNC HGNC:24300 HGNC
Ensembl ENSG00000173264 Ensembl
AllianceGenome HGNC:24300
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000438980.7 hg38 chr11 64,285,848 64,289,494 3,647
ENST00000411458.5 hg38 chr11 64,284,339 64,289,404 5,066
ENST00000377702.8 hg38 chr11 64,285,257 64,289,494 4,238
ENST00000313074.7 hg38 chr11 64,286,420 64,289,491 3,072
ENST00000411458.5 hg19 chr11 64,051,811 64,056,876 5,066
ENST00000313074.7 hg19 chr11 64,053,892 64,056,963 3,072
ENST00000377702.8 hg19 chr11 64,052,729 64,056,966 4,238
ENST00000438980.7 hg19 chr11 64,053,320 64,056,966 3,647
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