DUSP11 dual specificity phosphatase 11
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 8 |
Uncertain significance | 0 | 32 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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46 |
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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 | PIR1 |
MIM | 603092 OMIM |
HGNC | HGNC:3066 HGNC |
Ensembl | ENSG00000144048 Ensembl |
AllianceGenome | HGNC:3066 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000272444.8 | hg38 | chr2 | 73,762,213 | 73,780,103 | 17,891 |
ENST00000696055.1 | hg38 | chr2 | 73,762,415 | 73,780,103 | 17,689 |
ENST00000696053.1 | hg38 | chr2 | 73,762,260 | 73,780,103 | 17,844 |
ENST00000696052.1 | hg38 | chr2 | 73,762,227 | 73,780,092 | 17,866 |
ENST00000696056.1 | hg38 | chr2 | 73,762,431 | 73,780,103 | 17,673 |
ENST00000696057.1 | hg38 | chr2 | 73,773,253 | 73,780,111 | 6,859 |
ENST00000443070.5 | hg38 | chr2 | 73,767,419 | 73,780,121 | 12,703 |
ENST00000272444.8 | hg19 | chr2 | 73,989,340 | 74,007,230 | 17,891 |
ENST00000696052.1 | hg19 | chr2 | 73,989,354 | 74,007,219 | 17,866 |
ENST00000696053.1 | hg19 | chr2 | 73,989,387 | 74,007,230 | 17,844 |
ENST00000696055.1 | hg19 | chr2 | 73,989,542 | 74,007,230 | 17,689 |
ENST00000696056.1 | hg19 | chr2 | 73,989,558 | 74,007,230 | 17,673 |
ENST00000443070.5 | hg19 | chr2 | 73,994,546 | 74,007,248 | 12,703 |
ENST00000696057.1 | hg19 | chr2 | 74,000,380 | 74,007,238 | 6,859 |
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