OR2H2 olfactory receptor family 2 subfamily H member 2
Information
- Symbol
- OR2H2
- Type
- protein-coding
- Description
- olfactory receptor family 2 subfamily H member 2
- Entrez Gene ID
- 7932
- Genome
- hg19
- Position
- chr6:29,552,898-29,558,277
- Genome
- hg38
- Position
- chr6:29,585,121-29,590,500
- MIM
- 600578 OMIM
- HGNC
- HGNC:8253 HGNC
- Ensembl
- ENSG00000204657 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 24 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
26 |
 |
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 | FAT11 |
| SYNONYM | OLFR2 |
| SYNONYM | OLFR42B |
| SYNONYM | OR2H3 |
| SYNONYM | dJ271M21.2 |
| SYNONYM | hs6M1-12 |
| MIM | 600578 OMIM |
| HGNC | HGNC:8253 HGNC |
| Ensembl | ENSG00000204657 Ensembl |
| AllianceGenome | HGNC:8253 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000383640.4 | hg38 | chr6 | 29,587,455 | 29,588,968 | 1,514 |
| ENST00000641840.1 | hg38 | chr6 | 29,585,121 | 29,590,500 | 5,380 |
| ENST00000641840.1 | hg19 | chr6 | 29,552,898 | 29,558,277 | 5,380 |
| ENST00000383640.4 | hg19 | chr6 | 29,555,232 | 29,556,745 | 1,514 |
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