GPR85 G protein-coupled receptor 85
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
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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38 |
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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 |
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 | SREB |
SYNONYM | SREB2 |
MIM | 605188 OMIM |
HGNC | HGNC:4536 HGNC |
Ensembl | ENSG00000164604 Ensembl |
AllianceGenome | HGNC:4536 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000297146.7 | hg38 | chr7 | 113,080,247 | 113,087,755 | 7,509 |
ENST00000449591.2 | hg38 | chr7 | 113,082,285 | 113,086,167 | 3,883 |
ENST00000424100.2 | hg38 | chr7 | 113,082,285 | 113,086,827 | 4,543 |
ENST00000297146.7 | hg19 | chr7 | 112,720,302 | 112,727,810 | 7,509 |
ENST00000449591.2 | hg19 | chr7 | 112,722,340 | 112,726,222 | 3,883 |
ENST00000424100.2 | hg19 | chr7 | 112,722,340 | 112,726,882 | 4,543 |
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