ENSG00000160789 Expression In 33 Tumors

Ensembl ID Gene symbol Log2 Foldchange Pvaue Cancer
ENSG00000160789 0.61 8.78e-12 KIRC
ENSG00000160789 -0.7 3.55e-14 LUSC
ENSG00000160789 0.83 1.02e-15 LIHC
Ensembl ID Gene symbol Cancer types Pubmed ID
ENSG00000160789 colon cancer 12124339
ENSG00000160789 tumor 16809772
ENSG00000160789 skin cancer 16865251
ENSG00000160789 breast tumors 17550303
ENSG00000160789 tumour 18714339
ENSG00000160789 tumor 19680556
ENSG00000160789 tumor 20629083
ENSG00000160789 prostate cancer 20805891
ENSG00000160789 cancer 21106101
ENSG00000160789 tumours 21621406
ENSG00000160789 cancer 22068161
ENSG00000160789 tumor 23049808
ENSG00000160789 cancer 23666920
ENSG00000160789 Breast cancer 23820649
ENSG00000160789 cancer 24067370
ENSG00000160789 cancer 24637400
ENSG00000160789 tumor 24670416
ENSG00000160789 tumors 25490861
ENSG00000160789 tumor 26216294
ENSG00000160789 tumors 26439802
ENSG00000160789 metastatic colorectal cancer 26546295
ENSG00000160789 Metastatic Colorectal Cancer 26563355
ENSG00000160789 colon cancer 26716414
ENSG00000160789 tumor 26747892
ENSG00000160789 tumour 27843590
ENSG00000160789 tumors 27994771
ENSG00000160789 tumor 28188704
ENSG00000160789 soft tissue tumor 28851664
ENSG00000160789 tumors 28903424
ENSG00000160789 cancer 29405587
ENSG00000160789 cancer 29934494
ENSG00000160789 tumor 30134855
ENSG00000160789 neural tumor 30459475
ENSG00000160789 tumor 30613391
ENSG00000160789 tumour 30624546
ENSG00000160789 tumors 30686786
ENSG00000160789 pediatric tumor 30709876
ENSG00000160789 breast cancer 31311496
ENSG00000160789 cancers 31681438
Ensembl ID Gene symbol Disease/phenotype Mutation type Mutated / Total samples Literature
ENSG00000160789 melanocytic neoplasm gene_fusion 50.0% (9/18) 1 entry
ENSG00000160789 basal cell carcinoma sequence_alteration 5.172% (3/58) 1 entry
ENSG00000160789 colorectal adenocarcinoma sequence_alteration 2.724% (31/1138) 2 entries
ENSG00000160789 squamous cell lung carcinoma missense_variant 0.3937% (3/762) 1 entry
ENSG00000160789 HER2 Positive Breast Carcinoma missense_variant 4.63% (5/108) 1 entry
ENSG00000160789 ovarian serous adenocarcinoma sequence_alteration 0.7429% (5/673) 2 entries
ENSG00000160789 colon adenocarcinoma missense_variant 1.108% (8/722) 3 entries
ENSG00000160789 head and neck squamous cell carcinoma missense_variant 0.3195% (2/626) 1 entry
ENSG00000160789 colorectal adenocarcinoma stop_gained 2.724% (31/1138) 2 entries
ENSG00000160789 prostate carcinoma sequence_alteration 1.878% (8/426) 1 entry
ENSG00000160789 head and neck squamous cell carcinoma sequence_alteration 0.3195% (2/626) 1 entry
ENSG00000160789 colorectal adenocarcinoma missense_variant 2.724% (31/1138) 2 entries
ENSG00000160789 gastric adenocarcinoma missense_variant 1.075% (6/558) 1 entry
ENSG00000160789 melanoma sequence_alteration 3.96% (4/101) 2 entries
ENSG00000160789 melanoma missense_variant 3.96% (4/101) 2 entries
ENSG00000160789 rectal adenocarcinoma sequence_alteration 0.905% (2/221) 1 entry
ENSG00000160789 esophageal adenocarcinoma sequence_alteration 2.74% (12/438) 1 entry
ENSG00000160789 ovarian serous adenocarcinoma missense_variant 0.7429% (5/673) 1 entry
ENSG00000160789 prostate carcinoma missense_variant 1.878% (8/426) 1 entry
ENSG00000160789 lung adenocarcinoma missense_variant 0.258% (3/1163) 2 entries
ENSG00000160789 gastric intestinal type adenocarcinoma missense_variant 3.529% (3/85) 2 entries
ENSG00000160789 clear cell renal carcinoma sequence_alteration 0.155% (2/1290) 1 entry
ENSG00000160789 skin melanoma missense_variant 0.7239% (7/967) 1 entry
ENSG00000160789 colon adenocarcinoma sequence_alteration 1.108% (8/722) 3 entries
ENSG00000160789 bronchoalveolar adenocarcinoma sequence_alteration 4.545% (1/22) 1 entry
ENSG00000160789 esophageal squamous cell carcinoma missense_variant 0.7407% (5/675) 1 entry
ENSG00000160789 melanoma frameshift_variant 3.96% (4/101) 1 entry
ENSG00000160789 basal cell carcinoma missense_variant 5.172% (3/58) 1 entry
ENSG00000160789 colon carcinoma sequence_alteration 12.5% (1/8) 1 entry
ENSG00000160789 colorectal adenocarcinoma frameshift_variant 2.724% (31/1138) 1 entry
ENSG00000160789 Gallbladder Adenocarcinoma sequence_alteration 1.149% (1/87) 1 entry
ENSG00000160789 bronchoalveolar adenocarcinoma missense_variant 4.545% (1/22) 1 entry
ENSG00000160789 breast ductal adenocarcinoma missense_variant 5.822% (34/584) 1 entry
ENSG00000160789 colon carcinoma missense_variant 12.5% (1/8) 1 entry
ENSG00000160789 female breast carcinoma sequence_alteration 0.3745% (1/267) 1 entry
ENSG00000160789 acute myeloid leukemia missense_variant 0.441% (4/907) 1 entry
ENSG00000160789 diffuse large B-cell lymphoma missense_variant 0.33% (1/303) 1 entry
ENSG00000160789 Pancreatic Acinar Cell Carcinoma sequence_alteration 5.0% (1/20) 1 entry
Ensembl ID Gene symbol Cancer P-value Which worse show
ENSG00000160789 SARC 0.047 high
ENSG00000160789 UVM 0.024 high
ENSG00000160789 PAAD 0.018 high
ENSG00000160789 THCA 0.046 low
ENSG00000160789 ACC 0.00075 high
ENSG00000160789 LUSC 0.04 high
ENSG00000160789 READ 0.0087 high
ENSG00000160789 LUAD 0.0092 high
ENSG00000160789 BRCA 0.041 low
ENSG00000160789 COAD 0.034 high
ENSG00000160789 ESCA 0.0086 low
ENSG00000160789 OV 0.032 high
ENSG00000160789 DLBC 0.015 low
ENSG00000160789 PRAD 0.0028 low
ENSG00000160789 BLCA 0.027 high
ENSG00000160789 LAML 0.00013 high
ENSG00000160789 GBM 0.014 high
ENSG00000160789 SKCM 0.021 high
ENSG00000160789 LIHC 0.0038 high
Ensembl ID Gene symbol Cancer CNV type -log10(q-value) G-score average amplitude frequency
ENSG00000160789 CHOL Amp 0.963900 0.479130 0.983432 0.638889
ENSG00000160789 LUSC Amp 1.989044 0.235242 0.526091 0.522954
ENSG00000160789 LUAD Amp 15.388070 0.343773 0.582413 0.734496
ENSG00000160789 LGG Amp 0.918414 0.047055 0.554546 0.077973
ENSG00000160789 CESC Amp 2.920744 0.209523 0.630263 0.538983
ENSG00000160789 UCS Amp 4.936761 1.066062 1.001853 0.732143
ENSG00000160789 SARC Amp 1.930290 0.325917 0.655787 0.365759
ENSG00000160789 SKCM Amp 2.912439 0.187321 0.681499 0.544959
ENSG00000160789 LIHC Amp 17.883832 0.395614 0.908477 0.748649
ENSG00000160789 PCPG Amp 1.538300 0.086359 0.657410 0.166667
ENSG00000160789 DLBC Amp 1.852987 0.292853 0.670338 0.270833
ENSG00000160789 BLCA Amp 8.985118 0.370860 0.592638 0.450980
ENSG00000160789 BRCA Amp 17.692970 0.331403 0.778753 0.728704
ENSG00000160789 STAD Amp 1.897103 0.167330 0.462045 0.360544
ENSG00000160789 UCEC Amp 21.004709 0.362676 0.933568 0.476809
ENSG00000160789 OV Amp 12.550555 0.588800 0.752369 0.609672