OR9K2 olfactory receptor family 9 subfamily K member 2
Information
- Symbol
- OR9K2
- Type
- protein-coding
- Description
- olfactory receptor family 9 subfamily K member 2
- Entrez Gene ID
- 441639
- Genome
- hg19
- Position
- chr12:55,520,190-55,526,534
- Genome
- hg38
- Position
- chr12:55,126,406-55,132,750
- HGNC
- HGNC:15339 HGNC
- Ensembl
- ENSG00000170605 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 42 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
42 |
 |
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
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| 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
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| 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
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| 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 | OR12-2 |
| HGNC | HGNC:15339 HGNC |
| Ensembl | ENSG00000170605 Ensembl |
| AllianceGenome | HGNC:15339 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000641329.1 | hg38 | chr12 | 55,126,406 | 55,132,750 | 6,345 |
| ENST00000641374.1 | hg38 | chr12 | 55,129,681 | 55,130,802 | 1,122 |
| ENST00000641329.1 | hg19 | chr12 | 55,520,190 | 55,526,534 | 6,345 |
| ENST00000641374.1 | hg19 | chr12 | 55,523,465 | 55,524,586 | 1,122 |
Genome browser