DUSP14 dual specificity phosphatase 14
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 1 | 0 |
Uncertain significance | 0 | 24 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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24 |
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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
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 |
Search Word
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 | MKP-L |
SYNONYM | MKP6 |
MIM | 606618 OMIM |
HGNC | HGNC:17007 HGNC |
Ensembl | ENSG00000276023 Ensembl |
AllianceGenome | HGNC:17007 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000614411.1 | hg38 | chr17 | 37,509,879 | 37,513,501 | 3,623 |
ENST00000617516.5 | hg38 | chr17 | 37,489,891 | 37,513,498 | 23,608 |
ENST00000613659.1 | hg38 | chr17 | 37,491,464 | 37,513,487 | 22,024 |
ENST00000617516.5 | hg19 | chr17 | 35,849,997 | 35,873,600 | 23,604 |
ENST00000613659.1 | hg19 | chr17 | 35,851,570 | 35,873,589 | 22,020 |
ENST00000614411.1 | hg19 | chr17 | 35,869,981 | 35,873,603 | 3,623 |
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