GPR42 G protein-coupled receptor 42
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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4 |
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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 |
Prediction | |||||
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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 |
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SYNONYM | FFAR1L |
SYNONYM | FFAR3L |
SYNONYM | GPR41L |
SYNONYM | GPR42P |
MIM | 603822 OMIM |
HGNC | HGNC:4500 HGNC |
Ensembl | ENSG00000126251 Ensembl |
AllianceGenome | HGNC:4500 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000597214.1 | hg38 | chr19 | 35,371,290 | 35,372,471 | 1,182 |
ENST00000454971.3 | hg38 | chr19 | 35,371,068 | 35,372,962 | 1,895 |
ENST00000454971.3 | hg19 | chr19 | 35,861,970 | 35,863,864 | 1,895 |
ENST00000597214.1 | hg19 | chr19 | 35,862,192 | 35,863,373 | 1,182 |
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