OR2T33 olfactory receptor family 2 subfamily T member 33
Information
- Symbol
- OR2T33
- Type
- protein-coding
- Description
- olfactory receptor family 2 subfamily T member 33
- Entrez Gene ID
- 391195
- Genome
- hg19
- Position
- chr1:248,433,219-248,441,278
- Genome
- hg38
- Position
- chr1:248,269,917-248,277,976
- HGNC
- HGNC:31255 HGNC
- Ensembl
- ENSG00000177212 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 42 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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50 |
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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
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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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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 |
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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 | OR1-56 |
SYNONYM | OR2T32 |
HGNC | HGNC:31255 HGNC |
Ensembl | ENSG00000177212 Ensembl |
AllianceGenome | HGNC:31255 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000318021.4 | hg38 | chr1 | 248,272,771 | 248,273,836 | 1,066 |
ENST00000641220.1 | hg38 | chr1 | 248,269,917 | 248,277,976 | 8,060 |
ENST00000641220.1 | hg19 | chr1 | 248,433,219 | 248,441,278 | 8,060 |
ENST00000318021.4 | hg19 | chr1 | 248,436,073 | 248,437,138 | 1,066 |
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