SRXN1 sulfiredoxin 1
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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20 |
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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 |
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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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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 | C20orf139 |
SYNONYM | Npn3 |
SYNONYM | SRX |
SYNONYM | SRX1 |
MIM | 617583 OMIM |
HGNC | HGNC:16132 HGNC |
Ensembl | ENSG00000271303 Ensembl |
AllianceGenome | HGNC:16132 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000381962.4 | hg38 | chr20 | 646,615 | 653,200 | 6,586 |
ENST00000381962.4 | hg19 | chr20 | 627,259 | 633,844 | 6,586 |
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