GPR89B G protein-coupled receptor 89B
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 6 | 0 |
Uncertain significance | 0 | 18 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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18 |
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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
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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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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | GPHR |
SYNONYM | GPR89 |
SYNONYM | GPR89C |
SYNONYM | LINC02804 |
SYNONYM | SH120 |
SYNONYM | UNQ192 |
MIM | 612806 OMIM |
HGNC | HGNC:13840 HGNC |
Ensembl | ENSG00000188092 Ensembl |
AllianceGenome | HGNC:13840 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000314163.12 | hg38 | chr1 | 147,928,420 | 147,993,592 | 65,173 |
ENST00000314163.12 | hg19 | chr1 | 147,400,533 | 147,465,824 | 65,292 |
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