GPBAR1 G protein-coupled bile acid receptor 1
Information
- Symbol
- GPBAR1
- Type
- protein-coding
- Description
- G protein-coupled bile acid receptor 1
- Entrez Gene ID
- 151306
- Genome
- hg19
- Position
- chr2:219,125,738-219,128,582
- Genome
- hg38
- Position
- chr2:218,261,015-218,263,859
- MIM
- 610147 OMIM
- HGNC
- HGNC:19680 HGNC
- Ensembl
- ENSG00000179921 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 14 |
| Likely benign | 0 | 36 |
| Conflicting classifications of pathogenicity | 0 | 24 |
| Uncertain significance | 0 | 122 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
44 |
 |
122 |
 |
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
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | BG37 |
| SYNONYM | GPCR19 |
| SYNONYM | GPR131 |
| SYNONYM | M-BAR |
| SYNONYM | TGR5 |
| MIM | 610147 OMIM |
| HGNC | HGNC:19680 HGNC |
| Ensembl | ENSG00000179921 Ensembl |
| AllianceGenome | HGNC:19680 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000522678.5 | hg38 | chr2 | 218,261,015 | 218,263,859 | 2,845 |
| ENST00000519574.2 | hg38 | chr2 | 218,261,015 | 218,263,861 | 2,847 |
| ENST00000521462.1 | hg38 | chr2 | 218,261,034 | 218,263,848 | 2,815 |
| ENST00000479077.5 | hg38 | chr2 | 218,259,496 | 218,263,859 | 4,364 |
| ENST00000479077.5 | hg19 | chr2 | 219,124,219 | 219,128,582 | 4,364 |
| ENST00000522678.5 | hg19 | chr2 | 219,125,738 | 219,128,582 | 2,845 |
| ENST00000519574.2 | hg19 | chr2 | 219,125,738 | 219,128,584 | 2,847 |
| ENST00000521462.1 | hg19 | chr2 | 219,125,757 | 219,128,571 | 2,815 |
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