ADGRD1 adhesion G protein-coupled receptor D1
Information
- Symbol
- ADGRD1
- Type
- protein-coding
- Description
- adhesion G protein-coupled receptor D1
- Entrez Gene ID
- 283383
- Genome
- hg19
- Position
- chr12:131,438,981-131,623,833
- Genome
- hg38
- Position
- chr12:130,954,436-131,139,288
- MIM
- 613639 OMIM
- HGNC
- HGNC:19893 HGNC
- Ensembl
- ENSG00000111452 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 8 |
| Uncertain significance | 0 | 76 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
2 |
 |
82 |
 |
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 | GPR133 |
| SYNONYM | PGR25 |
| MIM | 613639 OMIM |
| HGNC | HGNC:19893 HGNC |
| Ensembl | ENSG00000111452 Ensembl |
| AllianceGenome | HGNC:19893 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000535015.5 | hg38 | chr12 | 130,954,436 | 131,139,288 | 184,853 |
| ENST00000543617.2 | hg38 | chr12 | 131,076,771 | 131,139,263 | 62,493 |
| ENST00000261654.10 | hg38 | chr12 | 130,953,907 | 131,141,469 | 187,563 |
| ENST00000335486.10 | hg38 | chr12 | 131,070,853 | 131,141,469 | 70,617 |
| ENST00000261654.10 | hg19 | chr12 | 131,438,452 | 131,626,014 | 187,563 |
| ENST00000535015.5 | hg19 | chr12 | 131,438,981 | 131,623,833 | 184,853 |
| ENST00000335486.10 | hg19 | chr12 | 131,555,398 | 131,626,014 | 70,617 |
| ENST00000543617.2 | hg19 | chr12 | 131,561,316 | 131,623,808 | 62,493 |
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