OXGR1 oxoglutarate receptor 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 6 |
Benign | 0 | 2 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 38 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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44 |
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6 |
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
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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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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 |
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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 | CAON2 |
SYNONYM | GPR80 |
SYNONYM | GPR99 |
SYNONYM | P2RY15 |
SYNONYM | P2Y15 |
SYNONYM | aKGR |
MIM | 606922 OMIM |
HGNC | HGNC:4531 HGNC |
Ensembl | ENSG00000165621 Ensembl |
AllianceGenome | HGNC:4531 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000543457.6 | hg38 | chr13 | 96,985,713 | 96,994,369 | 8,657 |
ENST00000541038.2 | hg38 | chr13 | 96,985,713 | 96,994,476 | 8,764 |
ENST00000298440.5 | hg38 | chr13 | 96,985,719 | 96,994,350 | 8,632 |
ENST00000543457.6 | hg19 | chr13 | 97,637,967 | 97,646,623 | 8,657 |
ENST00000541038.2 | hg19 | chr13 | 97,637,967 | 97,646,730 | 8,764 |
ENST00000298440.5 | hg19 | chr13 | 97,637,973 | 97,646,604 | 8,632 |
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