OR2B2 olfactory receptor family 2 subfamily B member 2
Information
- Symbol
- OR2B2
- Type
- protein-coding
- Description
- olfactory receptor family 2 subfamily B member 2
- Entrez Gene ID
- 81697
- Genome
- hg19
- Position
- chr6:27,878,963-27,880,174
- Genome
- hg38
- Position
- chr6:27,911,185-27,912,396
- HGNC
- HGNC:13966 HGNC
- Ensembl
- ENSG00000168131 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 34 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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36 |
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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
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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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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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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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 | OR2B2Q |
| SYNONYM | OR2B9 |
| SYNONYM | OR6-1 |
| SYNONYM | dJ193B12.4 |
| SYNONYM | hs6M1-10 |
| HGNC | HGNC:13966 HGNC |
| Ensembl | ENSG00000168131 Ensembl |
| AllianceGenome | HGNC:13966 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000303324.4 | hg38 | chr6 | 27,911,185 | 27,912,396 | 1,212 |
| ENST00000303324.4 | hg19 | chr6 | 27,878,963 | 27,880,174 | 1,212 |
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