HTR1B 5-hydroxytryptamine receptor 1B
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 14 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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18 |
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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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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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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 | 5-HT-1B |
SYNONYM | 5-HT-1D-beta |
SYNONYM | 5-HT1B |
SYNONYM | 5-HT1DB |
SYNONYM | HTR1D2 |
SYNONYM | HTR1DB |
SYNONYM | S12 |
MIM | 182131 OMIM |
HGNC | HGNC:5287 HGNC |
Ensembl | ENSG00000135312 Ensembl |
AllianceGenome | HGNC:5287 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000369947.5 | hg38 | chr6 | 77,460,924 | 77,463,491 | 2,568 |
ENST00000369947.5 | hg19 | chr6 | 78,170,641 | 78,173,208 | 2,568 |
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