DUSP4 dual specificity phosphatase 4
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 36 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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42 |
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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 | HVH2 |
SYNONYM | MKP-2 |
SYNONYM | MKP2 |
SYNONYM | TYP |
MIM | 602747 OMIM |
HGNC | HGNC:3070 HGNC |
Ensembl | ENSG00000120875 Ensembl |
AllianceGenome | HGNC:3070 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000240100.7 | hg38 | chr8 | 29,333,064 | 29,350,684 | 17,621 |
ENST00000240101.2 | hg38 | chr8 | 29,336,539 | 29,348,805 | 12,267 |
ENST00000240100.7 | hg19 | chr8 | 29,190,581 | 29,208,201 | 17,621 |
ENST00000240101.2 | hg19 | chr8 | 29,194,056 | 29,206,322 | 12,267 |
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