DUSP9 dual specificity phosphatase 9
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 4 |
not provided | 6 | 0 |
Uncertain significance | 0 | 42 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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50 |
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2 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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 |
Search Word
Target data | : |
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 | MKP-4 |
SYNONYM | MKP4 |
MIM | 300134 OMIM |
HGNC | HGNC:3076 HGNC |
Ensembl | ENSG00000130829 Ensembl |
AllianceGenome | HGNC:3076 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000342782.4 | hg38 | chrX | 153,647,203 | 153,651,326 | 4,124 |
ENST00000370167.8 | hg38 | chrX | 153,642,534 | 153,651,326 | 8,793 |
ENST00000370167.8 | hg19 | chrX | 152,907,988 | 152,916,781 | 8,794 |
ENST00000342782.4 | hg19 | chrX | 152,912,657 | 152,916,781 | 4,125 |
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