GPRC5A G protein-coupled receptor class C group 5 member A
Information
- Symbol
- GPRC5A
- Type
- protein-coding
- Description
- G protein-coupled receptor class C group 5 member A
- Entrez Gene ID
- 9052
- Genome
- hg19
- Position
- chr12:13,044,496-13,070,871
- Genome
- hg38
- Position
- chr12:12,891,562-12,917,937
- MIM
- 604138 OMIM
- HGNC
- HGNC:9836 HGNC
- Ensembl
- ENSG00000013588 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 10 |
| Uncertain significance | 0 | 36 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
48 |
 |
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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| 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 | GPCR5A |
| SYNONYM | PEIG-1 |
| SYNONYM | RAI3 |
| SYNONYM | RAIG1 |
| SYNONYM | TIG1 |
| MIM | 604138 OMIM |
| HGNC | HGNC:9836 HGNC |
| Ensembl | ENSG00000013588 Ensembl |
| AllianceGenome | HGNC:9836 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000014914.6 | hg38 | chr12 | 12,891,562 | 12,917,937 | 26,376 |
| ENST00000648791.1 | hg38 | chr12 | 12,908,244 | 12,913,411 | 5,168 |
| ENST00000713574.1 | hg38 | chr12 | 12,890,782 | 12,913,632 | 22,851 |
| ENST00000713574.1 | hg19 | chr12 | 13,043,716 | 13,066,566 | 22,851 |
| ENST00000014914.6 | hg19 | chr12 | 13,044,496 | 13,070,871 | 26,376 |
| ENST00000648791.1 | hg19 | chr12 | 13,061,178 | 13,066,345 | 5,168 |
| Key | Value |
|---|---|
| strand | + |
| UniProt | TSG |
| start | 13,043,955 |
| Gene Symbol | GPRC5A |
| Entrez GeneId | 9,052 |
| Chr Band | 12p13.1 |
| end | 13,066,600 |
| chr | chr12 |
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