DRD1 dopamine receptor D1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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30 |
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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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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 | D1R |
SYNONYM | DADR |
SYNONYM | DRD1A |
MIM | 126449 OMIM |
HGNC | HGNC:3020 HGNC |
Ensembl | ENSG00000184845 Ensembl |
AllianceGenome | HGNC:3020 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000393752.3 | hg38 | chr5 | 175,440,036 | 175,444,182 | 4,147 |
ENST00000393752.3 | hg19 | chr5 | 174,867,039 | 174,871,185 | 4,147 |
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