DUSP18 dual specificity phosphatase 18
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 34 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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34 |
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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 |
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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 | DSP18 |
SYNONYM | DUSP20 |
SYNONYM | LMWDSP20 |
MIM | 611446 OMIM |
HGNC | HGNC:18484 HGNC |
Ensembl | ENSG00000167065 Ensembl |
AllianceGenome | HGNC:18484 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000404885.5 | hg38 | chr22 | 30,652,051 | 30,667,843 | 15,793 |
ENST00000334679.4 | hg38 | chr22 | 30,661,445 | 30,667,875 | 6,431 |
ENST00000407308.1 | hg38 | chr22 | 30,652,051 | 30,667,860 | 15,810 |
ENST00000403268.1 | hg38 | chr22 | 30,661,445 | 30,667,855 | 6,411 |
ENST00000404885.5 | hg19 | chr22 | 31,048,038 | 31,063,830 | 15,793 |
ENST00000407308.1 | hg19 | chr22 | 31,048,038 | 31,063,847 | 15,810 |
ENST00000403268.1 | hg19 | chr22 | 31,057,432 | 31,063,842 | 6,411 |
ENST00000334679.4 | hg19 | chr22 | 31,057,432 | 31,063,862 | 6,431 |
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