ENSG00000091483 Expression In 33 Tumors

Ensembl ID Gene symbol Log2 Foldchange Pvaue Cancer
ENSG00000091483 -0.9 1.59e-36 KIRC
ENSG00000091483 0.57 1.21e-22 BRCA
ENSG00000091483 0.72 2.60e-11 KICH
ENSG00000091483 0.71 2.04e-19 LUSC
ENSG00000091483 0.85 3.57e-18 UCEC
ENSG00000091483 -1.9 3.76e-12 CHOL
ENSG00000091483 0.60 8.29e-16 LUAD
Ensembl ID Gene symbol Cancer types Pubmed ID
ENSG00000091483 renal cell cancer 12183404
ENSG00000091483 tumour 12761039
ENSG00000091483 cancer 15795514
ENSG00000091483 tumor 16206287
ENSG00000091483 cancer 16760265
ENSG00000091483 cancers 17111171
ENSG00000091483 tumors 17308357
ENSG00000091483 cancer 17960613
ENSG00000091483 tumor syndrome 18366737
ENSG00000091483 tumor 20109171
ENSG00000091483 tumor 20231875
ENSG00000091483 tumor 20354140
ENSG00000091483 cancer 20590333
ENSG00000091483 tumor 22645311
ENSG00000091483 tumors 23793769
ENSG00000091483 hereditary leiomyomatosis and renal cell cancer 24419633
ENSG00000091483 tumor 26983443
ENSG00000091483 hereditary leiomyomatosis and renal cell cancer syndrome 27454940
ENSG00000091483 cancer 27541980
ENSG00000091483 tumor 28094329
ENSG00000091483 tumour 28628081
ENSG00000091483 tumors 29315908
ENSG00000091483 Tumor 30090811
ENSG00000091483 renal cell cancer 30123928
ENSG00000091483 Lung Cancer 30683654
ENSG00000091483 tumor 31123043
Ensembl ID Gene symbol Disease/phenotype Mutation type Mutated / Total samples Literature
ENSG00000091483 prostate adenocarcinoma missense_variant 0.6515% (14/2149) 2 entries
ENSG00000091483 colorectal adenocarcinoma sequence_alteration 1.473% (17/1154) 1 entry
ENSG00000091483 esophageal squamous cell carcinoma missense_variant 0.8759% (6/685) 3 entries
ENSG00000091483 bladder transitional cell carcinoma missense_variant 0.6726% (3/446) 1 entry
ENSG00000091483 colon adenocarcinoma missense_variant 0.3123% (4/1281) 3 entries
ENSG00000091483 Mantle cell lymphoma sequence_alteration 3.774% (2/53) 1 entry
ENSG00000091483 clear cell renal carcinoma missense_variant 0.1894% (3/1584) 2 entries
ENSG00000091483 female breast carcinoma missense_variant 0.7491% (2/267) 1 entry
ENSG00000091483 renal cell carcinoma frameshift_variant 5.882% (4/68) 1 entry
ENSG00000091483 Endometrial Endometrioid Adenocarcinoma stop_gained 1.858% (12/646) 1 entry
ENSG00000091483 pancreatic ductal adenocarcinoma sequence_alteration 0.9512% (16/1682) 1 entry
ENSG00000091483 renal cell carcinoma missense_variant 5.882% (4/68) 1 entry
ENSG00000091483 melanoma missense_variant 2.759% (4/145) 2 entries
ENSG00000091483 lung carcinoma missense_variant 2.703% (3/111) 1 entry
ENSG00000091483 skin melanoma missense_variant 1.726% (20/1159) 4 entries
ENSG00000091483 rectal adenocarcinoma missense_variant 0.5495% (3/546) 1 entry
ENSG00000091483 acute myeloid leukemia sequence_alteration 0.3304% (3/908) 1 entry
ENSG00000091483 cecum adenocarcinoma missense_variant 0.7435% (2/269) 1 entry
ENSG00000091483 squamous cell lung carcinoma sequence_alteration 0.7511% (7/932) 1 entry
ENSG00000091483 breast ductal adenocarcinoma missense_variant 1.263% (20/1583) 1 entry
ENSG00000091483 hepatocellular carcinoma missense_variant 0.3049% (3/984) 2 entries
ENSG00000091483 brain glioblastoma missense_variant 0.2475% (3/1212) 1 entry
ENSG00000091483 lung adenocarcinoma sequence_alteration 1.034% (28/2709) 2 entries
ENSG00000091483 colorectal adenocarcinoma missense_variant 1.473% (17/1154) 1 entry
ENSG00000091483 lung adenocarcinoma missense_variant 1.034% (28/2709) 7 entries
ENSG00000091483 gastric adenocarcinoma missense_variant 0.5959% (5/839) 1 entry
ENSG00000091483 small cell lung carcinoma missense_variant 1.361% (6/441) 2 entries
ENSG00000091483 Endometrial Endometrioid Adenocarcinoma missense_variant 1.858% (12/646) 1 entry
ENSG00000091483 basal cell carcinoma sequence_alteration 4.412% (3/68) 1 entry
ENSG00000091483 squamous cell lung carcinoma missense_variant 0.7511% (7/932) 2 entries
ENSG00000091483 breast ductal adenocarcinoma sequence_alteration 1.263% (20/1583) 2 entries
ENSG00000091483 large cell lung carcinoma missense_variant 5.263% (1/19) 1 entry
ENSG00000091483 colorectal adenocarcinoma stop_gained 1.473% (17/1154) 1 entry
ENSG00000091483 gastric adenocarcinoma stop_gained 0.5959% (5/839) 1 entry
ENSG00000091483 non-small cell lung carcinoma missense_variant 1.042% (1/96) 1 entry
ENSG00000091483 esophageal squamous cell carcinoma stop_gained 0.8759% (6/685) 1 entry
ENSG00000091483 brain glioblastoma sequence_alteration 0.2475% (3/1212) 1 entry
ENSG00000091483 hemangioblastoma frameshift_variant 2.857% (1/35) 1 entry
ENSG00000091483 ovarian serous adenocarcinoma missense_variant 0.1196% (1/836) 1 entry
ENSG00000091483 oral squamous cell carcinoma missense_variant 0.3817% (1/262) 1 entry
ENSG00000091483 skin melanoma stop_gained 1.726% (20/1159) 1 entry
ENSG00000091483 papillary thyroid carcinoma stop_gained 0.409% (2/489) 1 entry
ENSG00000091483 gastric intestinal type adenocarcinoma missense_variant 1.176% (1/85) 1 entry
ENSG00000091483 bladder transitional cell carcinoma stop_gained 0.6726% (3/446) 1 entry
ENSG00000091483 pharyngeal squamous cell carcinoma missense_variant 1.235% (1/81) 1 entry
ENSG00000091483 basal cell carcinoma missense_variant 4.412% (3/68) 1 entry
ENSG00000091483 papillary thyroid carcinoma missense_variant 0.409% (2/489) 1 entry
ENSG00000091483 mucosal melanoma frameshift_variant 1.429% (1/70) 1 entry
ENSG00000091483 renal carcinoma sequence_alteration 5.0% (1/20) 1 entry
ENSG00000091483 nasopharyngeal squamous cell carcinoma missense_variant 0.5556% (1/180) 1 entry
ENSG00000091483 Thyroid Gland Undifferentiated (Anaplastic) Carcinoma missense_variant 0.7576% (2/264) 1 entry
ENSG00000091483 Brain Stem Glioblastoma sequence_alteration 1.786% (1/56) 1 entry
ENSG00000091483 lung adenocarcinoma amino_acid_insertion 1.034% (28/2709) 1 entry
ENSG00000091483 pancreatic neuroendocrine tumor missense_variant 0.8475% (2/236) 1 entry
ENSG00000091483 Gallbladder Adenocarcinoma sequence_alteration 0.6135% (1/163) 1 entry
ENSG00000091483 bile duct adenocarcinoma missense_variant 0.2597% (1/385) 1 entry
ENSG00000091483 esophageal adenocarcinoma missense_variant 0.7339% (4/545) 1 entry
ENSG00000091483 Thyroid Gland Undifferentiated (Anaplastic) Carcinoma conservative_inframe_deletion 0.7576% (2/264) 1 entry
ENSG00000091483 adrenocortical adenoma missense_variant 2.439% (1/41) 1 entry
ENSG00000091483 papillary renal cell carcinoma missense_variant 0.5168% (2/387) 1 entry
Ensembl ID Gene symbol Cancer P-value Which worse show
ENSG00000091483 STAD 0.047 high
ENSG00000091483 PAAD 0.014 low
ENSG00000091483 ACC 0.012 high
ENSG00000091483 KIRP 0.0011 low
ENSG00000091483 KICH 0.0013 high
ENSG00000091483 LUAD 0.019 high
ENSG00000091483 PCPG 0.004 high
ENSG00000091483 THYM 0.0075 high
ENSG00000091483 BRCA 0.018 high
ENSG00000091483 COAD 0.0065 low
ENSG00000091483 ESCA 0.006 high
ENSG00000091483 OV 0.0081 low
ENSG00000091483 KIRC 0.017 low
ENSG00000091483 BLCA 0.016 high
ENSG00000091483 LAML 0.0088 high
ENSG00000091483 SKCM 0.00034 high
ENSG00000091483 CESC 0.04 low
ENSG00000091483 LIHC 0.046 low
Ensembl ID Gene symbol Cancer CNV type -log10(q-value) G-score average amplitude frequency
ENSG00000091483 LUAD Amp 1.053615 0.126940 0.494673 0.680233
ENSG00000091483 CESC Amp 0.710411 0.128626 0.582079 0.508475
ENSG00000091483 SARC Del 5.597006 0.226640 0.498919 0.322957
ENSG00000091483 SKCM Amp 4.524225 0.230363 0.693031 0.550409
ENSG00000091483 LIHC Amp 5.972842 0.224277 0.848207 0.716216
ENSG00000091483 DLBC Del 1.810775 0.189464 0.584837 0.166667
ENSG00000091483 BRCA Amp 15.304201 0.311922 0.797473 0.733333
ENSG00000091483 UCEC Amp 1.324987 0.118649 0.840799 0.408163
ENSG00000091483 KIRC Del 0.673475 0.023991 0.458296 0.079545
ENSG00000091483 OV Amp 6.916039 0.490154 0.734395 0.533679