GPRC5D G protein-coupled receptor class C group 5 member D
Information
- Symbol
- GPRC5D
- Type
- protein-coding
- Description
- G protein-coupled receptor class C group 5 member D
- Entrez Gene ID
- 55507
- Genome
- hg19
- Position
- chr12:13,093,509-13,105,104
- Genome
- hg38
- Position
- chr12:12,940,575-12,952,170
- MIM
- 607437 OMIM
- HGNC
- HGNC:13310 HGNC
- Ensembl
- ENSG00000111291 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 42 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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48 |
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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
[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 |
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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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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 |
---|---|
MIM | 607437 OMIM |
HGNC | HGNC:13310 HGNC |
Ensembl | ENSG00000111291 Ensembl |
AllianceGenome | HGNC:13310 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000396333.3 | hg38 | chr12 | 12,940,842 | 12,950,384 | 9,543 |
ENST00000228887.6 | hg38 | chr12 | 12,940,575 | 12,952,170 | 11,596 |
ENST00000228887.6 | hg19 | chr12 | 13,093,509 | 13,105,104 | 11,596 |
ENST00000396333.3 | hg19 | chr12 | 13,093,776 | 13,103,318 | 9,543 |
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