TAAR2 trace amine associated receptor 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
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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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
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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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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 | GPR58 |
SYNONYM | taR-2 |
MIM | 604849 OMIM |
HGNC | HGNC:4514 HGNC |
Ensembl | ENSG00000146378 Ensembl |
AllianceGenome | HGNC:4514 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000275191.2 | hg38 | chr6 | 132,617,022 | 132,618,178 | 1,157 |
ENST00000367931.1 | hg38 | chr6 | 132,617,150 | 132,624,275 | 7,126 |
ENST00000275191.2 | hg19 | chr6 | 132,938,161 | 132,939,317 | 1,157 |
ENST00000367931.1 | hg19 | chr6 | 132,938,289 | 132,945,414 | 7,126 |
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