OR2H1 olfactory receptor family 2 subfamily H member 1
Information
- Symbol
- OR2H1
- Type
- protein-coding
- Description
- olfactory receptor family 2 subfamily H member 1
- Entrez Gene ID
- 26716
- Genome
- hg19
- Position
- chr6:29,424,932-29,432,105
- Genome
- hg38
- Position
- chr6:29,457,155-29,464,328
- HGNC
- HGNC:8252 HGNC
- Ensembl
- ENSG00000204688 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 8 |
| not provided | 1 | 0 |
| Uncertain significance | 0 | 30 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
38 |
 |
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
| 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 | 6M1-16 |
| SYNONYM | HS6M1-16 |
| SYNONYM | OLFR42A-9004-14 |
| SYNONYM | OLFR42A-9004.14/9026.2 |
| SYNONYM | OR2H6 |
| SYNONYM | OR2H8 |
| SYNONYM | OR6-2 |
| SYNONYM | dJ994E9.4 |
| HGNC | HGNC:8252 HGNC |
| Ensembl | ENSG00000204688 Ensembl |
| AllianceGenome | HGNC:8252 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000377133.6 | hg38 | chr6 | 29,457,155 | 29,464,328 | 7,174 |
| ENST00000377132.1 | hg38 | chr6 | 29,459,771 | 29,464,328 | 4,558 |
| ENST00000377136.5 | hg38 | chr6 | 29,457,181 | 29,464,328 | 7,148 |
| ENST00000396792.2 | hg38 | chr6 | 29,461,440 | 29,462,733 | 1,294 |
| ENST00000377133.6 | hg19 | chr6 | 29,424,932 | 29,432,105 | 7,174 |
| ENST00000377136.5 | hg19 | chr6 | 29,424,958 | 29,432,105 | 7,148 |
| ENST00000377132.1 | hg19 | chr6 | 29,427,548 | 29,432,105 | 4,558 |
| ENST00000396792.2 | hg19 | chr6 | 29,429,217 | 29,430,510 | 1,294 |
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