ENSG00000127914 Expression In 33 Tumors

Ensembl ID Gene symbol Log2 Foldchange Pvaue Cancer
ENSG00000127914 -0.7 4.64e-16 KIRC
ENSG00000127914 -1.1 6.15e-16 COAD
Ensembl ID Gene symbol Cancer types Pubmed ID
ENSG00000127914 thyroid cancer 15630448
ENSG00000127914 thyroid tumors 15753649
ENSG00000127914 breast cancer 18334708
ENSG00000127914 colorectal cancer 18619730
ENSG00000127914 thyroid cancer 19766698
ENSG00000127914 cancer 20106900
ENSG00000127914 breast cancer 21931171
ENSG00000127914 cancer 22833545
ENSG00000127914 thyroid cancer 22887574
ENSG00000127914 Lung Cancer 23762359
ENSG00000127914 cancer 23807220
ENSG00000127914 cancer 24668645
ENSG00000127914 thyroid cancer 24868250
ENSG00000127914 breast cancer 24943594
ENSG00000127914 tumor 25446987
ENSG00000127914 cancer 25469175
ENSG00000127914 cancer 25733820
ENSG00000127914 Colorectal Cancers 26786868
ENSG00000127914 colorectal cancer 26887056
ENSG00000127914 colorectal cancer 27039663
ENSG00000127914 tumor 27270325
ENSG00000127914 colorectal cancer 27686732
ENSG00000127914 colorectal cancer 27888635
ENSG00000127914 Prostate cancer 28108736
ENSG00000127914 tumor 28127051
ENSG00000127914 breast cancer 28210903
ENSG00000127914 primary cancer 28327965
ENSG00000127914 cancer 28524162
ENSG00000127914 tumor 29433456
ENSG00000127914 tumors 29464327
ENSG00000127914 Colorectal cancer 29739426
ENSG00000127914 tumors 30754153
Ensembl ID Gene symbol Disease/phenotype Mutation type Mutated / Total samples Literature
ENSG00000127914 prostate carcinoma missense_variant 3.299% (16/485) 3 entries
ENSG00000127914 colorectal adenocarcinoma stop_gained 9.861% (128/1298) 3 entries
ENSG00000127914 esophageal adenocarcinoma missense_variant 13.01% (57/438) 2 entries
ENSG00000127914 papillary renal cell carcinoma stop_gained 1.194% (4/335) 1 entry
ENSG00000127914 cecum adenocarcinoma frameshift_variant 9.848% (13/132) 1 entry
ENSG00000127914 gastric intestinal type adenocarcinoma missense_variant 9.412% (8/85) 2 entries
ENSG00000127914 prostate adenocarcinoma frameshift_variant 6.121% (89/1454) 1 entry
ENSG00000127914 nasopharyngeal squamous cell carcinoma missense_variant 2.395% (4/167) 2 entries
ENSG00000127914 Parathyroid Gland Carcinoma missense_variant 15.79% (3/19) 1 entry
ENSG00000127914 Breast Carcinoma by Gene Expression Profile missense_variant 10.53% (2/19) 2 entries
ENSG00000127914 cecum adenocarcinoma missense_variant 9.848% (13/132) 2 entries
ENSG00000127914 prostate adenocarcinoma sequence_alteration 6.121% (89/1454) 2 entries
ENSG00000127914 ovarian serous adenocarcinoma missense_variant 1.189% (8/673) 2 entries
ENSG00000127914 skin melanoma missense_variant 6.722% (65/967) 5 entries
ENSG00000127914 colon adenocarcinoma sequence_alteration 7.403% (57/770) 3 entries
ENSG00000127914 head and neck squamous cell carcinoma amino_acid_insertion 2.236% (14/626) 1 entry
ENSG00000127914 clear cell renal carcinoma frameshift_variant 2.54% (35/1378) 2 entries
ENSG00000127914 colorectal adenocarcinoma frameshift_variant 9.861% (128/1298) 5 entries
ENSG00000127914 bile duct adenocarcinoma missense_variant 1.058% (2/189) 2 entries
ENSG00000127914 small cell lung carcinoma missense_variant 2.469% (8/324) 1 entry
ENSG00000127914 clear cell renal carcinoma missense_variant 2.54% (35/1378) 4 entries
ENSG00000127914 lung adenocarcinoma stop_gained 4.095% (50/1221) 1 entry
ENSG00000127914 brain glioblastoma amino_acid_insertion 0.9719% (9/926) 1 entry
ENSG00000127914 basal cell carcinoma missense_variant 8.621% (5/58) 1 entry
ENSG00000127914 colon adenocarcinoma stop_gained 7.403% (57/770) 3 entries
ENSG00000127914 female breast carcinoma missense_variant 1.79% (7/391) 2 entries
ENSG00000127914 HER2 Positive Breast Carcinoma missense_variant 7.104% (13/183) 2 entries
ENSG00000127914 clear cell renal carcinoma sequence_alteration 2.54% (35/1378) 2 entries
ENSG00000127914 bladder transitional cell carcinoma missense_variant 2.19% (3/137) 1 entry
ENSG00000127914 melanoma frameshift_variant 11.88% (12/101) 1 entry
ENSG00000127914 Cervical Small Cell Carcinoma missense_variant 33.33% (2/6) 1 entry
ENSG00000127914 melanoma stop_gained 11.88% (12/101) 1 entry
ENSG00000127914 gastric intestinal type adenocarcinoma frameshift_variant 9.412% (8/85) 1 entry
ENSG00000127914 cecum adenocarcinoma stop_gained 9.848% (13/132) 1 entry
ENSG00000127914 lung adenocarcinoma missense_variant 4.095% (50/1221) 7 entries
ENSG00000127914 colon adenocarcinoma frameshift_variant 7.403% (57/770) 4 entries
ENSG00000127914 breast ductal adenocarcinoma sequence_alteration 13.78% (85/617) 2 entries
ENSG00000127914 breast carcinoma missense_variant 1.983% (28/1412) 3 entries
ENSG00000127914 lung adenocarcinoma sequence_alteration 4.095% (50/1221) 2 entries
ENSG00000127914 prostate carcinoma frameshift_variant 3.299% (16/485) 2 entries
ENSG00000127914 papillary renal cell carcinoma missense_variant 1.194% (4/335) 1 entry
ENSG00000127914 small cell lung carcinoma frameshift_variant 2.469% (8/324) 2 entries
ENSG00000127914 esophageal adenocarcinoma frameshift_variant 13.01% (57/438) 1 entry
ENSG00000127914 melanoma sequence_alteration 11.88% (12/101) 1 entry
ENSG00000127914 gastric adenocarcinoma missense_variant 4.418% (30/679) 2 entries
ENSG00000127914 prostate adenocarcinoma missense_variant 6.121% (89/1454) 3 entries
ENSG00000127914 skin melanoma stop_gained 6.722% (65/967) 1 entry
ENSG00000127914 melanoma missense_variant 11.88% (12/101) 1 entry
ENSG00000127914 colorectal adenocarcinoma conservative_inframe_deletion 9.861% (128/1298) 2 entries
ENSG00000127914 colorectal adenocarcinoma sequence_alteration 9.861% (128/1298) 4 entries
ENSG00000127914 colon adenocarcinoma missense_variant 7.403% (57/770) 8 entries
ENSG00000127914 hepatocellular carcinoma missense_variant 2.32% (21/905) 1 entry
ENSG00000127914 central nervous system primitive neuroectodermal neoplasm missense_variant 2.477% (11/444) 2 entries
ENSG00000127914 squamous cell lung carcinoma sequence_alteration 3.152% (26/825) 1 entry
ENSG00000127914 gastric adenocarcinoma stop_gained 4.418% (30/679) 1 entry
ENSG00000127914 Thyroid Gland Oncocytic Follicular Carcinoma gene_fusion 47.5% (19/40) 1 entry
ENSG00000127914 oral squamous cell carcinoma missense_variant 4.762% (10/210) 4 entries
ENSG00000127914 pancreatic ductal adenocarcinoma missense_variant 5.242% (66/1259) 2 entries
ENSG00000127914 breast ductal adenocarcinoma missense_variant 13.78% (85/617) 2 entries
ENSG00000127914 squamous cell lung carcinoma missense_variant 3.152% (26/825) 4 entries
ENSG00000127914 prostate carcinoma sequence_alteration 3.299% (16/485) 1 entry
ENSG00000127914 alveolar rhabdomyosarcoma missense_variant 3.39% (2/59) 1 entry
ENSG00000127914 diffuse large B-cell lymphoma missense_variant 1.967% (6/305) 3 entries
ENSG00000127914 colorectal adenocarcinoma missense_variant 9.861% (128/1298) 6 entries
ENSG00000127914 Endometrial Endometrioid Adenocarcinoma missense_variant 6.534% (36/551) 1 entry
ENSG00000127914 metaplastic breast carcinoma missense_variant 3.922% (2/51) 1 entry
ENSG00000127914 brain glioblastoma missense_variant 0.9719% (9/926) 1 entry
ENSG00000127914 rectal adenocarcinoma missense_variant 3.493% (8/229) 4 entries
ENSG00000127914 papillary thyroid carcinoma gene_fusion 49.81% (265/532) 2 entries
ENSG00000127914 endometrial carcinoma missense_variant 8.696% (2/23) 2 entries
ENSG00000127914 esophageal squamous cell carcinoma missense_variant 3.102% (21/677) 6 entries
ENSG00000127914 esophageal adenocarcinoma sequence_alteration 13.01% (57/438) 1 entry
ENSG00000127914 head and neck squamous cell carcinoma sequence_alteration 2.236% (14/626) 1 entry
ENSG00000127914 hemangioblastoma frameshift_variant 10.0% (1/10) 1 entry
ENSG00000127914 neoplasm missense_variant 10.71% (3/28) 1 entry
ENSG00000127914 pseudomyxoma peritonei stop_gained 10.0% (1/10) 1 entry
ENSG00000127914 small cell lung carcinoma sequence_alteration 2.469% (8/324) 1 entry
ENSG00000127914 lung carcinoid tumor missense_variant 9.091% (1/11) 1 entry
ENSG00000127914 colorectal adenocarcinoma amino_acid_insertion 9.861% (128/1298) 1 entry
ENSG00000127914 diffuse large B-cell lymphoma stop_gained 1.967% (6/305) 1 entry
ENSG00000127914 female breast carcinoma conservative_inframe_deletion 1.79% (7/391) 1 entry
ENSG00000127914 T-cell acute lymphoblastic leukemia stop_gained 0.2632% (1/380) 1 entry
ENSG00000127914 Extraskeletal Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor missense_variant 3.704% (1/27) 1 entry
ENSG00000127914 non-small cell lung carcinoma missense_variant 1.613% (1/62) 1 entry
ENSG00000127914 Parathyroid Gland Carcinoma stop_gained 15.79% (3/19) 1 entry
ENSG00000127914 brain glioblastoma frameshift_variant 0.9719% (9/926) 1 entry
ENSG00000127914 Gallbladder Adenocarcinoma sequence_alteration 1.786% (2/112) 1 entry
ENSG00000127914 basal cell carcinoma sequence_alteration 8.621% (5/58) 1 entry
ENSG00000127914 polycythemia vera missense_variant 2.083% (1/48) 1 entry
ENSG00000127914 Merkel cell skin cancer missense_variant 6.667% (2/30) 1 entry
ENSG00000127914 gastric adenocarcinoma frameshift_variant 4.418% (30/679) 1 entry
ENSG00000127914 Gallbladder Adenocarcinoma missense_variant 1.786% (2/112) 1 entry
ENSG00000127914 breast ductal adenocarcinoma frameshift_variant 13.78% (85/617) 1 entry
ENSG00000127914 ovarian serous adenocarcinoma amino_acid_insertion 1.189% (8/673) 1 entry
ENSG00000127914 Ampulla of Vater Carcinoma missense_variant 1.176% (1/85) 1 entry
ENSG00000127914 Merkel cell skin cancer sequence_alteration 6.667% (2/30) 1 entry
ENSG00000127914 rectal adenocarcinoma stop_gained 3.493% (8/229) 1 entry
ENSG00000127914 colon carcinoma missense_variant 12.5% (1/8) 1 entry
ENSG00000127914 head and neck squamous cell carcinoma missense_variant 2.236% (14/626) 1 entry
ENSG00000127914 adenosquamous lung carcinoma missense_variant 18.18% (2/11) 1 entry
ENSG00000127914 adenosquamous lung carcinoma stop_gained 18.18% (2/11) 1 entry
ENSG00000127914 gastric intestinal type adenocarcinoma stop_gained 9.412% (8/85) 1 entry
ENSG00000127914 oral squamous cell carcinoma stop_gained 4.762% (10/210) 1 entry
ENSG00000127914 large cell lung carcinoma missense_variant 5.556% (1/18) 1 entry
ENSG00000127914 chondrosarcoma missense_variant 50.0% (1/2) 1 entry
ENSG00000127914 diffuse gastric adenocarcinoma missense_variant 1.266% (1/79) 1 entry
ENSG00000127914 meningioma (disease) missense_variant 2.041% (1/49) 1 entry
ENSG00000127914 ovarian serous adenocarcinoma stop_gained 1.189% (8/673) 1 entry
ENSG00000127914 rectal adenocarcinoma sequence_alteration 3.493% (8/229) 1 entry
ENSG00000127914 chromophobe renal cell carcinoma frameshift_variant 0.8696% (1/115) 1 entry
ENSG00000127914 skin carcinoma stop_gained 4.808% (5/104) 1 entry
ENSG00000127914 Pleural Epithelioid Mesothelioma frameshift_variant 2.128% (2/94) 1 entry
ENSG00000127914 Pleural Epithelioid Mesothelioma amino_acid_insertion 2.128% (2/94) 1 entry
ENSG00000127914 Invasive Breast Carcinoma missense_variant 2.174% (1/46) 1 entry
ENSG00000127914 ovarian neoplasm missense_variant 1.724% (1/58) 1 entry
Ensembl ID Gene symbol Cancer P-value Which worse show
ENSG00000127914 MESO 0.011 low
ENSG00000127914 CHOL 0.033 low
ENSG00000127914 UVM 0.03 high
ENSG00000127914 PAAD 0.045 low
ENSG00000127914 UCEC 0.0051 high
ENSG00000127914 LUSC 0.011 low
ENSG00000127914 KIRP 0.01 low
ENSG00000127914 LUAD 0.023 low
ENSG00000127914 ESCA 0.0094 high
ENSG00000127914 DLBC 0.047 high
ENSG00000127914 KIRC 0.00058 low
ENSG00000127914 PRAD 0.038 high
ENSG00000127914 BLCA 0.016 high
ENSG00000127914 LIHC 0.033 high
Ensembl ID Gene symbol Cancer CNV type -log10(q-value) G-score average amplitude frequency
ENSG00000127914 LUSC Amp 3.075342 0.263526 0.559049 0.524950
ENSG00000127914 KIRP Amp 0.909495 0.059421 0.915985 0.604167
ENSG00000127914 GBM Amp 1.328051 0.079324 0.788997 0.828423
ENSG00000127914 PAAD Amp 1.403195 0.105568 0.447415 0.304348
ENSG00000127914 ESCA Amp 10.795111 0.694197 0.788847 0.619565
ENSG00000127914 HNSC Amp 7.496573 0.242342 0.636350 0.318008
ENSG00000127914 LIHC Amp 2.066124 0.147769 0.650865 0.332432
ENSG00000127914 TGCT Amp 1.190440 0.140338 0.532682 0.773333
ENSG00000127914 STAD Amp 22.957906 0.512527 0.792171 0.460317
ENSG00000127914 PRAD Amp 1.385337 0.055934 0.507048 0.215447