ADGRG4 adhesion G protein-coupled receptor G4
Information
- Symbol
- ADGRG4
- Type
- protein-coding
- Description
- adhesion G protein-coupled receptor G4
- Entrez Gene ID
- 139378
- Genome
- hg19
- Position
- chrX:135,383,122-135,499,049
- Genome
- hg38
- Position
- chrX:136,300,963-136,416,890
- MIM
- 301085 OMIM
- HGNC
- HGNC:18992 HGNC
- Ensembl
- ENSG00000156920 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 60 |
Conflicting classifications of pathogenicity | 0 | 6 |
not provided | 6 | 0 |
Uncertain significance | 0 | 250 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
2 |
![]() |
310 |
![]() |
2 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
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
|
Category | : |
|
Search word | : | |
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
|
Category | : |
|
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 | GPR112 |
SYNONYM | PGR17 |
SYNONYM | RP1-299I16 |
MIM | 301085 OMIM |
HGNC | HGNC:18992 HGNC |
Ensembl | ENSG00000156920 Ensembl |
AllianceGenome | HGNC:18992 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000370652.5 | hg38 | chrX | 136,304,853 | 136,416,888 | 112,036 |
ENST00000394143.6 | hg38 | chrX | 136,300,963 | 136,416,890 | 115,928 |
ENST00000394141.1 | hg38 | chrX | 136,306,021 | 136,416,684 | 110,664 |
ENST00000394143.6 | hg19 | chrX | 135,383,122 | 135,499,049 | 115,928 |
ENST00000370652.5 | hg19 | chrX | 135,387,012 | 135,499,047 | 112,036 |
ENST00000394141.1 | hg19 | chrX | 135,388,180 | 135,498,843 | 110,664 |
Genome browser