OR51E1 olfactory receptor family 51 subfamily E member 1
Information
- Symbol
- OR51E1
- Type
- protein-coding
- Description
- olfactory receptor family 51 subfamily E member 1
- Entrez Gene ID
- 143503
- Genome
- hg19
- Position
- chr11:4,665,212-4,676,718
- Genome
- hg38
- Position
- chr11:4,643,982-4,655,488
- MIM
- 611267 OMIM
- HGNC
- HGNC:15194 HGNC
- Ensembl
- ENSG00000180785 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 6 |
| Uncertain significance | 0 | 46 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
52 |
 |
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
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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 | D-GPCR |
| SYNONYM | DGPCR |
| SYNONYM | GPR136 |
| SYNONYM | GPR164 |
| SYNONYM | OR51E1P |
| SYNONYM | OR52A3P |
| SYNONYM | POGR |
| SYNONYM | PSGR2 |
| MIM | 611267 OMIM |
| HGNC | HGNC:15194 HGNC |
| Ensembl | ENSG00000180785 Ensembl |
| AllianceGenome | HGNC:15194 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000530215.2 | hg38 | chr11 | 4,643,420 | 4,655,488 | 12,069 |
| ENST00000396952.6 | hg38 | chr11 | 4,643,982 | 4,655,488 | 11,507 |
| ENST00000530215.2 | hg19 | chr11 | 4,664,650 | 4,676,718 | 12,069 |
| ENST00000396952.6 | hg19 | chr11 | 4,665,212 | 4,676,718 | 11,507 |
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