OR2W3 olfactory receptor family 2 subfamily W member 3
Information
- Symbol
- OR2W3
- Type
- protein-coding
- Description
- olfactory receptor family 2 subfamily W member 3
- Entrez Gene ID
- 343171
- Genome
- hg19
- Position
- chr1:248,058,889-248,059,833
- Genome
- hg38
- Position
- chr1:247,895,587-247,896,531
- MIM
- 616729 OMIM
- HGNC
- HGNC:15021 HGNC
- Ensembl
- ENSG00000238243 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 42 |
Likely benign | 0 | 98 |
Conflicting classifications of pathogenicity | 0 | 4 |
Uncertain significance | 0 | 262 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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30 |
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372 |
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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 |
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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 | |||
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | OR2W3P |
SYNONYM | OR2W8P |
SYNONYM | OST718 |
MIM | 616729 OMIM |
HGNC | HGNC:15021 HGNC |
Ensembl | ENSG00000238243 Ensembl |
AllianceGenome | HGNC:15021 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000360358.3 | hg38 | chr1 | 247,895,587 | 247,896,531 | 945 |
ENST00000360358.3 | hg19 | chr1 | 248,058,889 | 248,059,833 | 945 |
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