GPR101 G protein-coupled receptor 101
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 2 |
Benign | 0 | 26 |
Likely benign | 0 | 28 |
Conflicting classifications of pathogenicity | 0 | 6 |
not provided | 6 | 0 |
Uncertain significance | 0 | 46 |
Ranking
ClinVar | |
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0 |
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0 |
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10 |
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80 |
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4 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
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 |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
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 |
Search Word
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 | GPCR6 |
SYNONYM | PAGH2 |
SYNONYM | PITA2 |
MIM | 300393 OMIM |
HGNC | HGNC:14963 HGNC |
Ensembl | ENSG00000165370 Ensembl |
AllianceGenome | HGNC:14963 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000651716.2 | hg38 | chrX | 137,023,929 | 137,033,995 | 10,067 |
ENST00000651716.2 | hg19 | chrX | 136,106,088 | 136,116,154 | 10,067 |
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