OR2M2 olfactory receptor family 2 subfamily M member 2
Information
- Symbol
- OR2M2
- Type
- protein-coding
- Description
- olfactory receptor family 2 subfamily M member 2
- Entrez Gene ID
- 391194
- Genome
- hg19
- Position
- chr1:248,338,123-248,344,369
- Genome
- hg38
- Position
- chr1:248,174,821-248,181,067
- HGNC
- HGNC:8268 HGNC
- Ensembl
- ENSG00000198601 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 48 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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58 |
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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 |
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SYNONYM | OR2M2Q |
SYNONYM | OST423 |
HGNC | HGNC:8268 HGNC |
Ensembl | ENSG00000198601 Ensembl |
AllianceGenome | HGNC:8268 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000641211.1 | hg38 | chr1 | 248,174,821 | 248,181,067 | 6,247 |
ENST00000641836.1 | hg38 | chr1 | 248,174,821 | 248,181,067 | 6,247 |
ENST00000641211.1 | hg19 | chr1 | 248,338,123 | 248,344,369 | 6,247 |
ENST00000641836.1 | hg19 | chr1 | 248,338,123 | 248,344,369 | 6,247 |
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