OR52N5 olfactory receptor family 52 subfamily N member 5
Information
- Symbol
- OR52N5
- Type
- protein-coding
- Description
- olfactory receptor family 52 subfamily N member 5
- Entrez Gene ID
- 390075
- Genome
- hg19
- Position
- chr11:5,797,395-5,804,585
- Genome
- hg38
- Position
- chr11:5,776,165-5,783,355
- HGNC
- HGNC:15231 HGNC
- Ensembl
- ENSG00000181009 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
Uncertain significance | 0 | 28 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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36 |
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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 |
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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 | OR11-62 |
SYNONYM | OR52N5Q |
HGNC | HGNC:15231 HGNC |
Ensembl | ENSG00000181009 Ensembl |
AllianceGenome | HGNC:15231 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000317093.2 | hg38 | chr11 | 5,777,634 | 5,778,667 | 1,034 |
ENST00000641181.1 | hg38 | chr11 | 5,776,165 | 5,783,355 | 7,191 |
ENST00000641181.1 | hg19 | chr11 | 5,797,395 | 5,804,585 | 7,191 |
ENST00000317093.2 | hg19 | chr11 | 5,798,864 | 5,799,897 | 1,034 |
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