HRH4 histamine receptor H4
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 36 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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40 |
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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 | AXOR35 |
SYNONYM | BG26 |
SYNONYM | GPCR105 |
SYNONYM | GPRv53 |
SYNONYM | H4 |
SYNONYM | H4R |
SYNONYM | HH4R |
MIM | 606792 OMIM |
HGNC | HGNC:17383 HGNC |
Ensembl | ENSG00000134489 Ensembl |
AllianceGenome | HGNC:17383 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000256906.5 | hg38 | chr18 | 24,460,637 | 24,479,961 | 19,325 |
ENST00000426880.2 | hg38 | chr18 | 24,460,729 | 24,477,562 | 16,834 |
ENST00000256906.5 | hg19 | chr18 | 22,040,601 | 22,059,925 | 19,325 |
ENST00000426880.2 | hg19 | chr18 | 22,040,693 | 22,057,526 | 16,834 |
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