GPR155 G protein-coupled receptor 155
Information
- Symbol
- GPR155
- Type
- protein-coding
- Description
- G protein-coupled receptor 155
- Entrez Gene ID
- 151556
- Genome
- hg19
- Position
- chr2:175,296,299-175,351,757
- Genome
- hg38
- Position
- chr2:174,431,571-174,487,029
- HGNC
- HGNC:22951 HGNC
- Ensembl
- ENSG00000163328 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 8 |
| Likely benign | 0 | 6 |
| Uncertain significance | 0 | 84 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
98 |
 |
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
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| Filtering | : |
| 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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| Category | : |
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| Search word | : | |
| Filtering | : |
| 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 | DEP.7 |
| SYNONYM | DEPDC3 |
| SYNONYM | LYCHOS |
| SYNONYM | PGR22 |
| HGNC | HGNC:22951 HGNC |
| Ensembl | ENSG00000163328 Ensembl |
| AllianceGenome | HGNC:22951 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000295500.8 | hg38 | chr2 | 174,435,144 | 174,487,037 | 51,894 |
| ENST00000614352.4 | hg38 | chr2 | 174,431,571 | 174,487,088 | 55,518 |
| ENST00000392552.7 | hg38 | chr2 | 174,431,571 | 174,487,029 | 55,459 |
| ENST00000392551.6 | hg38 | chr2 | 174,434,152 | 174,487,094 | 52,943 |
| ENST00000392552.7 | hg19 | chr2 | 175,296,299 | 175,351,757 | 55,459 |
| ENST00000614352.4 | hg19 | chr2 | 175,296,299 | 175,351,816 | 55,518 |
| ENST00000392551.6 | hg19 | chr2 | 175,298,880 | 175,351,822 | 52,943 |
| ENST00000295500.8 | hg19 | chr2 | 175,299,872 | 175,351,765 | 51,894 |
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