PLXDC1 plexin domain containing 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 64 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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66 |
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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
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 |
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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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | TEM3 |
SYNONYM | TEM7 |
MIM | 606826 OMIM |
HGNC | HGNC:20945 HGNC |
Ensembl | ENSG00000161381 Ensembl |
AllianceGenome | HGNC:20945 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000315392.9 | hg38 | chr17 | 39,063,313 | 39,151,637 | 88,325 |
ENST00000444911.6 | hg38 | chr17 | 39,067,160 | 39,152,699 | 85,540 |
ENST00000315392.9 | hg19 | chr17 | 37,219,566 | 37,307,890 | 88,325 |
ENST00000444911.6 | hg19 | chr17 | 37,223,413 | 37,308,952 | 85,540 |
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