ENSG00000091483 Expression In 33 Tumors

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