OR1F1 olfactory receptor family 1 subfamily F member 1
Information
- Symbol
- OR1F1
- Type
- protein-coding
- Description
- olfactory receptor family 1 subfamily F member 1
- Entrez Gene ID
- 4992
- Genome
- hg19
- Position
- chr16:3,238,204-3,256,556
- Genome
- hg38
- Position
- chr16:3,188,204-3,206,556
- MIM
- 603232 OMIM
- HGNC
- HGNC:8194 HGNC
- Ensembl
- ENSG00000168124 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 6 |
| Likely benign | 0 | 6 |
| Uncertain significance | 0 | 42 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
52 |
 |
2 |
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 | |||||||||||
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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 | OLFMF |
| SYNONYM | OR16-36 |
| SYNONYM | OR16-37 |
| SYNONYM | OR16-88 |
| SYNONYM | OR16-89 |
| SYNONYM | OR16-90 |
| SYNONYM | OR1F10 |
| SYNONYM | OR1F13P |
| SYNONYM | OR1F4 |
| SYNONYM | OR1F5 |
| SYNONYM | OR1F6 |
| SYNONYM | OR1F7 |
| SYNONYM | OR1F8 |
| SYNONYM | OR1F9 |
| SYNONYM | OR3-145 |
| SYNONYM | ORL1023 |
| MIM | 603232 OMIM |
| HGNC | HGNC:8194 HGNC |
| Ensembl | ENSG00000168124 Ensembl |
| AllianceGenome | HGNC:8194 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000304646.3 | hg38 | chr16 | 3,188,204 | 3,206,556 | 18,353 |
| ENST00000304646.3 | hg19 | chr16 | 3,238,204 | 3,256,556 | 18,353 |
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