DUSP11 dual specificity phosphatase 11

Information
Symbol
DUSP11
Type
protein-coding
Description
dual specificity phosphatase 11
Entrez Gene ID
8446
Genome
hg19
Position
chr2:73,989,340-74,007,230
Genome
hg38
Position
chr2:73,762,213-73,780,103
MIM
603092 OMIM
HGNC
HGNC:3066 HGNC
Ensembl
ENSG00000144048 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 8
Uncertain significance 0 32
Ranking
ClinVar
0
0
0
46
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
Category :
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Variant name Gene AA change CDS Japanese
frequency
TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence
Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM PIR1
MIM 603092 OMIM
HGNC HGNC:3066 HGNC
Ensembl ENSG00000144048 Ensembl
AllianceGenome HGNC:3066
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
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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