ENSG00000163399 Expression In 33 Tumors

Ensembl ID Gene symbol Log2 Foldchange Pvaue Cancer
ENSG00000163399 -2.7 6.50e-183 KIRC
ENSG00000163399 -1.8 1.70e-30 KIRP
ENSG00000163399 0.93 6.75e-14 UCEC
ENSG00000163399 2.64 4.80e-14 CHOL
Ensembl ID Gene symbol Cancer types Pubmed ID
ENSG00000163399 cancer 20460749
ENSG00000163399 tumor 23409748
ENSG00000163399 tumor 23946277
ENSG00000163399 tumors 24399884
ENSG00000163399 tumor 24561634
ENSG00000163399 tumors 24739312
ENSG00000163399 tumor 24817817
ENSG00000163399 cancer 25161250
ENSG00000163399 GBM 25400117
ENSG00000163399 tumors 26285814
ENSG00000163399 Tumors 26334094
ENSG00000163399 tumor 26739091
ENSG00000163399 tumors 26815163
ENSG00000163399 cancer 27431571
ENSG00000163399 cancer 27701467
ENSG00000163399 tumor 27845894
ENSG00000163399 tumors 28484360
ENSG00000163399 breast cancer 28529692
ENSG00000163399 lung cancer 29117117
ENSG00000163399 tumor 29309535
ENSG00000163399 tumors 29416716
ENSG00000163399 tumors 29594118
ENSG00000163399 tumor 29653366
ENSG00000163399 tumor 30015972
ENSG00000163399 cancer 30202019
ENSG00000163399 tumours 31000732
ENSG00000163399 GBM 31114755
ENSG00000163399 tumor 31207362
ENSG00000163399 Cancer 31324856
ENSG00000163399 tumor 31789380
Ensembl ID Gene symbol Disease/phenotype Mutation type Mutated / Total samples Literature
ENSG00000163399 colorectal adenocarcinoma frameshift_variant 3.163% (36/1138) 1 entry
ENSG00000163399 colorectal adenocarcinoma sequence_alteration 3.163% (36/1138) 1 entry
ENSG00000163399 aldosterone-producing adenoma missense_variant 4.888% (63/1289) 10 entries
ENSG00000163399 colorectal adenocarcinoma missense_variant 3.163% (36/1138) 2 entries
ENSG00000163399 aldosterone-producing adenoma conservative_inframe_deletion 4.888% (63/1289) 5 entries
ENSG00000163399 female breast carcinoma missense_variant 0.7491% (2/267) 1 entry
ENSG00000163399 prostate carcinoma sequence_alteration 1.171% (5/427) 1 entry
ENSG00000163399 breast carcinoma missense_variant 1.205% (17/1411) 1 entry
ENSG00000163399 melanoma missense_variant 2.97% (3/101) 2 entries
ENSG00000163399 lung adenocarcinoma sequence_alteration 0.8598% (10/1163) 2 entries
ENSG00000163399 colorectal adenocarcinoma stop_gained 3.163% (36/1138) 1 entry
ENSG00000163399 prostate adenocarcinoma sequence_alteration 0.9629% (14/1454) 2 entries
ENSG00000163399 pancreatic ductal adenocarcinoma missense_variant 1.112% (14/1259) 1 entry
ENSG00000163399 breast ductal adenocarcinoma sequence_alteration 2.74% (16/584) 2 entries
ENSG00000163399 squamous cell lung carcinoma missense_variant 0.3937% (3/762) 1 entry
ENSG00000163399 colon adenocarcinoma missense_variant 1.801% (13/722) 4 entries
ENSG00000163399 small cell lung carcinoma missense_variant 1.258% (4/318) 2 entries
ENSG00000163399 esophageal squamous cell carcinoma sequence_alteration 0.4444% (3/675) 1 entry
ENSG00000163399 skin carcinoma missense_variant 2.885% (3/104) 1 entry
ENSG00000163399 lung adenocarcinoma missense_variant 0.8598% (10/1163) 4 entries
ENSG00000163399 aldosterone-producing adenoma frameshift_variant 4.888% (63/1289) 1 entry
ENSG00000163399 clear cell renal carcinoma sequence_alteration 0.7323% (9/1229) 1 entry
ENSG00000163399 brain glioblastoma sequence_alteration 0.7559% (7/926) 1 entry
ENSG00000163399 skin melanoma missense_variant 1.034% (10/967) 3 entries
ENSG00000163399 colon adenocarcinoma frameshift_variant 1.801% (13/722) 2 entries
ENSG00000163399 gastric intestinal type adenocarcinoma missense_variant 4.706% (4/85) 2 entries
ENSG00000163399 esophageal adenocarcinoma missense_variant 1.598% (7/438) 1 entry
ENSG00000163399 rectal adenocarcinoma missense_variant 0.905% (2/221) 1 entry
ENSG00000163399 papillary renal cell carcinoma missense_variant 0.9009% (3/333) 1 entry
ENSG00000163399 colon adenocarcinoma stop_gained 1.801% (13/722) 2 entries
ENSG00000163399 chronic lymphocytic leukemia missense_variant 0.2252% (2/888) 1 entry
ENSG00000163399 osteosarcoma missense_variant 0.8621% (1/116) 1 entry
ENSG00000163399 neoplasm missense_variant 3.571% (1/28) 1 entry
ENSG00000163399 anaplastic astrocytoma missense_variant 2.273% (1/44) 1 entry
ENSG00000163399 colon adenocarcinoma sequence_alteration 1.801% (13/722) 1 entry
ENSG00000163399 breast ductal adenocarcinoma stop_gained 2.74% (16/584) 1 entry
ENSG00000163399 Merkel cell skin cancer sequence_alteration 3.333% (1/30) 1 entry
ENSG00000163399 small cell lung carcinoma stop_gained 1.258% (4/318) 1 entry
ENSG00000163399 prostate carcinoma missense_variant 1.171% (5/427) 1 entry
ENSG00000163399 breast phyllodes tumor frameshift_variant 4.545% (1/22) 1 entry
ENSG00000163399 gastric intestinal type adenocarcinoma frameshift_variant 4.706% (4/85) 1 entry
ENSG00000163399 Pleural Epithelioid Mesothelioma conservative_inframe_deletion 1.064% (1/94) 1 entry
ENSG00000163399 esophageal squamous cell carcinoma missense_variant 0.4444% (3/675) 1 entry
ENSG00000163399 chronic myelomonocytic leukemia missense_variant 3.704% (1/27) 1 entry
ENSG00000163399 ovarian serous adenocarcinoma missense_variant 0.1486% (1/673) 1 entry
ENSG00000163399 oral squamous cell carcinoma sequence_alteration 0.4878% (1/205) 1 entry
ENSG00000163399 melanoma sequence_alteration 2.97% (3/101) 1 entry
ENSG00000163399 basal cell carcinoma missense_variant 1.724% (1/58) 1 entry
ENSG00000163399 prostate carcinoma frameshift_variant 1.171% (5/427) 1 entry
ENSG00000163399 skin melanoma sequence_alteration 1.034% (10/967) 1 entry
ENSG00000163399 bile duct adenocarcinoma missense_variant 0.5291% (1/189) 1 entry
ENSG00000163399 oral squamous cell carcinoma missense_variant 0.4878% (1/205) 1 entry
Ensembl ID Gene symbol Cancer P-value Which worse show
ENSG00000163399 MESO 0.001 low
ENSG00000163399 PAAD 0.0043 high
ENSG00000163399 UCEC 0.019 high
ENSG00000163399 THCA 0.024 high
ENSG00000163399 ACC 0.04 low
ENSG00000163399 READ 0.014 low
ENSG00000163399 KIRP 0.0014 low
ENSG00000163399 THYM 0.048 high
ENSG00000163399 ESCA 0.00026 low
ENSG00000163399 BLCA 0.00039 high
ENSG00000163399 LAML 0.0012 high
ENSG00000163399 SKCM 0.033 low
ENSG00000163399 LIHC 0.00022 high
Ensembl ID Gene symbol Cancer CNV type -log10(q-value) G-score average amplitude frequency
ENSG00000163399 LUSC Del 16.311682 0.188869 0.416526 0.445110
ENSG00000163399 LUAD Del 11.826767 0.138688 0.355057 0.294574
ENSG00000163399 CESC Del 1.299537 0.079272 0.429588 0.108475
ENSG00000163399 COAD Del 2.191960 0.058093 0.424371 0.252772
ENSG00000163399 PAAD Amp 2.166355 0.129659 0.705406 0.092391
ENSG00000163399 ESCA Del 2.788554 0.152983 0.408036 0.326087
ENSG00000163399 SKCM Del 2.846441 0.097940 0.434524 0.201635
ENSG00000163399 HNSC Del 17.629880 0.160531 0.411495 0.250958
ENSG00000163399 PCPG Del 16.867986 0.259301 0.700825 0.697531
ENSG00000163399 DLBC Del 1.497111 0.171420 0.504331 0.208333
ENSG00000163399 BRCA Del 3.170040 0.082402 0.387298 0.261111
ENSG00000163399 STAD Del 2.631997 0.085925 0.369738 0.204082
ENSG00000163399 MESO Del 5.204096 0.273774 0.573953 0.321839