NOXO1 NADPH oxidase organizer 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
Uncertain significance | 0 | 76 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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84 |
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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 | P41NOX |
SYNONYM | P41NOXA |
SYNONYM | P41NOXB |
SYNONYM | P41NOXC |
SYNONYM | SH3PXD5 |
SYNONYM | SNX28 |
MIM | 611256 OMIM |
HGNC | HGNC:19404 HGNC |
Ensembl | ENSG00000196408 Ensembl |
AllianceGenome | HGNC:19404 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000354249.8 | hg38 | chr16 | 1,978,917 | 1,981,549 | 2,633 |
ENST00000566005.5 | hg38 | chr16 | 1,979,040 | 1,981,183 | 2,144 |
ENST00000397280.8 | hg38 | chr16 | 1,979,040 | 1,981,183 | 2,144 |
ENST00000356120.9 | hg38 | chr16 | 1,978,917 | 1,981,469 | 2,553 |
ENST00000356120.9 | hg19 | chr16 | 2,028,918 | 2,031,470 | 2,553 |
ENST00000354249.8 | hg19 | chr16 | 2,028,918 | 2,031,550 | 2,633 |
ENST00000397280.8 | hg19 | chr16 | 2,029,041 | 2,031,184 | 2,144 |
ENST00000566005.5 | hg19 | chr16 | 2,029,041 | 2,031,184 | 2,144 |
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