OR2A12 olfactory receptor family 2 subfamily A member 12
Information
- Symbol
- OR2A12
- Type
- protein-coding
- Description
- olfactory receptor family 2 subfamily A member 12
- Entrez Gene ID
- 346525
- Genome
- hg19
- Position
- chr7:143,783,371-143,796,046
- Genome
- hg38
- Position
- chr7:144,086,278-144,098,953
- HGNC
- HGNC:15082 HGNC
- Ensembl
- ENSG00000221858 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
22 |
![]() |
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 | OR2A12P |
SYNONYM | OR2A16P |
HGNC | HGNC:15082 HGNC |
Ensembl | ENSG00000221858 Ensembl |
AllianceGenome | HGNC:15082 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000408949.2 | hg38 | chr7 | 144,095,048 | 144,096,093 | 1,046 |
ENST00000641592.1 | hg38 | chr7 | 144,086,278 | 144,098,953 | 12,676 |
ENST00000641592.1 | hg19 | chr7 | 143,783,371 | 143,796,046 | 12,676 |
ENST00000408949.2 | hg19 | chr7 | 143,792,141 | 143,793,186 | 1,046 |
Genome browser