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ENSG00000182054 Expression In 33 Tumors
ACC
BLCA
BRCA
CESC
CHOL
COAD
DLBC
ESCA
GBM
HNSC
KICH
KIRC
KIRP
LAML
LGG
LIHC
LUAD
LUSC
MESO
OV
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PCPG
PRAD
READ
SARC
SKCM
STAD
TGCT
THCA
THYM
UCEC
UCS
UVM
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ACC
BLCA
BRCA
CESC
CHOL
COAD
DLBC
ESCA
GBM
HNSC
KICH
KIRC
KIRP
LAML
LGG
LIHC
LUAD
LUSC
MESO
OV
PAAD
PCPG
PRAD
READ
SARC
SKCM
STAD
TGCT
THCA
THYM
UCEC
UCS
UVM
FPKM
plotly-logomark
Show
10
20
50
entries
Search:
Ensembl ID
Gene symbol
Log2 Foldchange
Pvaue
Cancer
ENSG00000182054
IDH2
-1.0
7.09e-31
KIRC
ENSG00000182054
IDH2
-1.1
8.00e-22
HNSC
ENSG00000182054
IDH2
1.43
9.80e-58
BRCA
ENSG00000182054
IDH2
1.30
7.19e-37
LUSC
ENSG00000182054
IDH2
-1.3
5.72e-15
KIRP
ENSG00000182054
IDH2
2.18
3.17e-51
UCEC
ENSG00000182054
IDH2
1.17
2.88e-25
LUAD
Showing 1 to 7 of 7 entries
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KIRC
HNSC
BRCA
LUSC
KIRP
UCEC
LUAD
0
200
400
600
800
1000
1200
tumor
normal
plotly-logomark
Show
10
20
50
entries
Search:
Ensembl ID
Gene symbol
Cancer types
Pubmed ID
ENSG00000182054
IDH2
tumors
19228619
ENSG00000182054
IDH2
tumors
19554337
ENSG00000182054
IDH2
tumor
19765000
ENSG00000182054
IDH2
tumors
19915015
ENSG00000182054
IDH2
tumors
19996293
ENSG00000182054
IDH2
tumors
20130071
ENSG00000182054
IDH2
tumor
20131059
ENSG00000182054
IDH2
AML
20142433
ENSG00000182054
IDH2
Cancer
20160062
ENSG00000182054
IDH2
thyroid cancer
20171178
Showing 1 to 10 of 613 entries
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1
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62
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entries
Search:
Ensembl ID
Gene symbol
Disease/phenotype
Mutation type
Mutated / Total samples
Literature
ENSG00000182054
IDH2
myelodysplastic syndrome
sequence_alteration
3.981% (135/3391)
13 entries
ENSG00000182054
IDH2
Sinonasal Undifferentiated Carcinoma
missense_variant
78.95% (15/19)
2 entries
ENSG00000182054
IDH2
myelodysplastic syndrome
missense_variant
3.981% (135/3391)
26 entries
ENSG00000182054
IDH2
angioimmunoblastic T-cell lymphoma
missense_variant
23.99% (95/396)
11 entries
ENSG00000182054
IDH2
angioimmunoblastic T-cell lymphoma
sequence_alteration
23.99% (95/396)
9 entries
ENSG00000182054
IDH2
anaplastic oligodendroglioma
sequence_alteration
6.03% (36/597)
7 entries
ENSG00000182054
IDH2
acute myeloid leukemia
missense_variant
9.39% (1465/15602)
74 entries
ENSG00000182054
IDH2
anaplastic oligodendroglioma
missense_variant
6.03% (36/597)
15 entries
ENSG00000182054
IDH2
acute myeloid leukemia
sequence_alteration
9.39% (1465/15602)
46 entries
ENSG00000182054
IDH2
myeloproliferative disorder
missense_variant
1.748% (5/286)
4 entries
Showing 1 to 10 of 168 entries
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Search:
Ensembl ID
Gene symbol
Cancer
P-value
Which worse
show
ENSG00000182054
IDH2
BLCA
0.013
high
show
ENSG00000182054
IDH2
BRCA
0.011
low
show
ENSG00000182054
IDH2
CHOL
0.041
high
show
ENSG00000182054
IDH2
COAD
0.05
low
show
ENSG00000182054
IDH2
LIHC
0.047
low
show
ENSG00000182054
IDH2
LUAD
0.022
low
show
ENSG00000182054
IDH2
LUSC
0.0058
low
show
ENSG00000182054
IDH2
MESO
0.0019
high
show
ENSG00000182054
IDH2
OV
0.027
low
show
ENSG00000182054
IDH2
PRAD
0.027
low
show
Showing 1 to 10 of 14 entries
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Search:
Ensembl ID
Gene symbol
Cancer
CNV type
-log10(q-value)
G-score
average amplitude
frequency
ENSG00000182054
IDH2
LUSC
Amp
1.857290
0.231492
0.464070
0.339321
ENSG00000182054
IDH2
CESC
Amp
1.847321
0.173523
0.555277
0.254237
ENSG00000182054
IDH2
SKCM
Amp
3.184817
0.194604
0.525253
0.324251
ENSG00000182054
IDH2
BRCA
Amp
2.855060
0.183291
0.619195
0.166667
ENSG00000182054
IDH2
STAD
Amp
10.622433
0.337963
0.666877
0.251701
ENSG00000182054
IDH2
OV
Amp
0.602498
0.322412
0.654058
0.240069
Showing 1 to 6 of 6 entries
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