GPR34 G protein-coupled receptor 34
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 4 |
| Likely benign | 0 | 2 |
| not provided | 6 | 0 |
| Uncertain significance | 0 | 8 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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2 |
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10 |
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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
Locus Zoom
Variants
Search Word
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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 | |||||||||||
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | LPS1 |
| SYNONYM | LYPSR1 |
| MIM | 300241 OMIM |
| HGNC | HGNC:4490 HGNC |
| Ensembl | ENSG00000171659 Ensembl |
| AllianceGenome | HGNC:4490 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000649219.1 | hg38 | chrX | 41,689,051 | 41,697,161 | 8,111 |
| ENST00000378138.5 | hg38 | chrX | 41,689,006 | 41,697,273 | 8,268 |
| ENST00000378142.9 | hg38 | chrX | 41,688,973 | 41,697,275 | 8,303 |
| ENST00000378142.9 | hg19 | chrX | 41,548,226 | 41,556,528 | 8,303 |
| ENST00000378138.5 | hg19 | chrX | 41,548,259 | 41,556,526 | 8,268 |
| ENST00000649219.1 | hg19 | chrX | 41,548,304 | 41,556,414 | 8,111 |
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