GPX1 glutathione peroxidase 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 10 |
Uncertain significance | 0 | 58 |
Ranking
ClinVar | |
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0 |
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0 |
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6 |
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62 |
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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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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 | GPXD |
SYNONYM | GSHPX1 |
MIM | 138320 OMIM |
HGNC | HGNC:4553 HGNC |
Ensembl | ENSG00000233276 Ensembl |
AllianceGenome | HGNC:4553 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000496791.3 | hg38 | chr3 | 49,357,176 | 49,358,325 | 1,150 |
ENST00000704356.1 | hg38 | chr3 | 49,357,179 | 49,358,325 | 1,147 |
ENST00000703796.1 | hg38 | chr3 | 49,357,176 | 49,358,284 | 1,109 |
ENST00000703795.1 | hg38 | chr3 | 49,357,174 | 49,358,605 | 1,432 |
ENST00000643797.2 | hg38 | chr3 | 49,357,176 | 49,358,353 | 1,178 |
ENST00000646881.3 | hg38 | chr3 | 49,357,176 | 49,358,377 | 1,202 |
ENST00000419783.3 | hg38 | chr3 | 49,357,176 | 49,358,353 | 1,178 |
ENST00000704376.1 | hg38 | chr3 | 49,357,179 | 49,358,323 | 1,145 |
ENST00000704375.1 | hg38 | chr3 | 49,357,176 | 49,358,353 | 1,178 |
ENST00000704378.1 | hg38 | chr3 | 49,357,179 | 49,358,325 | 1,147 |
ENST00000704377.1 | hg38 | chr3 | 49,357,179 | 49,358,325 | 1,147 |
ENST00000704374.1 | hg38 | chr3 | 49,357,176 | 49,358,322 | 1,147 |
ENST00000419349.3 | hg38 | chr3 | 49,357,176 | 49,358,323 | 1,148 |
ENST00000703795.1 | hg19 | chr3 | 49,394,607 | 49,396,038 | 1,432 |
ENST00000703796.1 | hg19 | chr3 | 49,394,609 | 49,395,717 | 1,109 |
ENST00000704374.1 | hg19 | chr3 | 49,394,609 | 49,395,755 | 1,147 |
ENST00000419349.3 | hg19 | chr3 | 49,394,609 | 49,395,756 | 1,148 |
ENST00000496791.3 | hg19 | chr3 | 49,394,609 | 49,395,758 | 1,150 |
ENST00000419783.3 | hg19 | chr3 | 49,394,609 | 49,395,786 | 1,178 |
ENST00000643797.2 | hg19 | chr3 | 49,394,609 | 49,395,786 | 1,178 |
ENST00000704375.1 | hg19 | chr3 | 49,394,609 | 49,395,786 | 1,178 |
ENST00000646881.3 | hg19 | chr3 | 49,394,609 | 49,395,810 | 1,202 |
ENST00000704376.1 | hg19 | chr3 | 49,394,612 | 49,395,756 | 1,145 |
ENST00000704356.1 | hg19 | chr3 | 49,394,612 | 49,395,758 | 1,147 |
ENST00000704377.1 | hg19 | chr3 | 49,394,612 | 49,395,758 | 1,147 |
ENST00000704378.1 | hg19 | chr3 | 49,394,612 | 49,395,758 | 1,147 |
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