CD63 CD63 molecule
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Uncertain significance | 0 | 14 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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16 |
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2 |
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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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 |
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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 | AD1 |
SYNONYM | HOP-26 |
SYNONYM | ME491 |
SYNONYM | MLA1 |
SYNONYM | OMA81H |
SYNONYM | Pltgp40 |
SYNONYM | TSPAN30 |
MIM | 155740 OMIM |
HGNC | HGNC:1692 HGNC |
Ensembl | ENSG00000135404 Ensembl |
AllianceGenome | HGNC:1692 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000546939.5 | hg38 | chr12 | 55,725,470 | 55,727,900 | 2,431 |
ENST00000420846.7 | hg38 | chr12 | 55,725,443 | 55,728,650 | 3,208 |
ENST00000552067.5 | hg38 | chr12 | 55,725,448 | 55,727,128 | 1,681 |
ENST00000549117.5 | hg38 | chr12 | 55,725,482 | 55,729,707 | 4,226 |
ENST00000548160.5 | hg38 | chr12 | 55,725,470 | 55,727,059 | 1,590 |
ENST00000257857.9 | hg38 | chr12 | 55,725,323 | 55,729,009 | 3,687 |
ENST00000548898.5 | hg38 | chr12 | 55,725,323 | 55,727,108 | 1,786 |
ENST00000552754.5 | hg38 | chr12 | 55,725,535 | 55,728,349 | 2,815 |
ENST00000552692.5 | hg38 | chr12 | 55,725,470 | 55,728,482 | 3,013 |
ENST00000550776.5 | hg38 | chr12 | 55,725,546 | 55,727,815 | 2,270 |
ENST00000548898.5 | hg19 | chr12 | 56,119,107 | 56,120,892 | 1,786 |
ENST00000257857.9 | hg19 | chr12 | 56,119,107 | 56,122,793 | 3,687 |
ENST00000420846.7 | hg19 | chr12 | 56,119,227 | 56,122,434 | 3,208 |
ENST00000552067.5 | hg19 | chr12 | 56,119,232 | 56,120,912 | 1,681 |
ENST00000548160.5 | hg19 | chr12 | 56,119,254 | 56,120,843 | 1,590 |
ENST00000546939.5 | hg19 | chr12 | 56,119,254 | 56,121,684 | 2,431 |
ENST00000552692.5 | hg19 | chr12 | 56,119,254 | 56,122,266 | 3,013 |
ENST00000549117.5 | hg19 | chr12 | 56,119,266 | 56,123,491 | 4,226 |
ENST00000552754.5 | hg19 | chr12 | 56,119,319 | 56,122,133 | 2,815 |
ENST00000550776.5 | hg19 | chr12 | 56,119,330 | 56,121,599 | 2,270 |
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