OR2N1P olfactory receptor family 2 subfamily N member 1 pseudogene
Information
- Symbol
- OR2N1P
- Type
- pseudo
- Description
- olfactory receptor family 2 subfamily N member 1 pseudogene
- Entrez Gene ID
- 26701
- Genome
- hg19
- Position
- chr6:29,105,657-29,106,593
- Genome
- hg38
- Position
- chr6:29,137,880-29,138,816
- HGNC
- HGNC:8271 HGNC
- Ensembl
- ENSG00000203492 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
 |
0 |
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0 |
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0 |
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0 |
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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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| 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 | |||
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| 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 | HS6M1-2 |
| SYNONYM | OLFR89 |
| SYNONYM | OR6-7 |
| HGNC | HGNC:8271 HGNC |
| Ensembl | ENSG00000203492 Ensembl |
| AllianceGenome | HGNC:8271 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000421799.1 | hg38 | chr6 | 29,137,880 | 29,138,816 | 937 |
| ENST00000421799.1 | hg19 | chr6 | 29,105,657 | 29,106,593 | 937 |
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