GPR55 G protein-coupled receptor 55
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 44 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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46 |
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2 |
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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | LPIR1 |
MIM | 604107 OMIM |
HGNC | HGNC:4511 HGNC |
Ensembl | ENSG00000135898 Ensembl |
AllianceGenome | HGNC:4511 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000622008.4 | hg38 | chr2 | 230,907,319 | 230,925,226 | 17,908 |
ENST00000650999.1 | hg38 | chr2 | 230,907,328 | 230,925,242 | 17,915 |
ENST00000392040.5 | hg38 | chr2 | 230,907,328 | 230,925,226 | 17,899 |
ENST00000392039.2 | hg38 | chr2 | 230,909,866 | 230,961,066 | 51,201 |
ENST00000622008.4 | hg19 | chr2 | 231,772,034 | 231,789,941 | 17,908 |
ENST00000392040.5 | hg19 | chr2 | 231,772,043 | 231,789,941 | 17,899 |
ENST00000650999.1 | hg19 | chr2 | 231,772,043 | 231,789,957 | 17,915 |
ENST00000392039.2 | hg19 | chr2 | 231,774,581 | 231,825,781 | 51,201 |
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