MRC2 mannose receptor C-type 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 146 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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154 |
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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 |
Prediction | |||||
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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 | CD280 |
SYNONYM | CLEC13E |
SYNONYM | ENDO180 |
SYNONYM | UPARAP |
MIM | 612264 OMIM |
HGNC | HGNC:16875 HGNC |
Ensembl | ENSG00000011028 Ensembl |
AllianceGenome | HGNC:16875 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000446119.2 | hg38 | chr17 | 62,681,458 | 62,693,595 | 12,138 |
ENST00000303375.10 | hg38 | chr17 | 62,627,670 | 62,693,597 | 65,928 |
ENST00000303375.10 | hg19 | chr17 | 60,705,031 | 60,770,958 | 65,928 |
ENST00000446119.2 | hg19 | chr17 | 60,758,819 | 60,770,956 | 12,138 |
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