ENSG00000105568 Expression In 33 Tumors

Ensembl ID Gene symbol Log2 Foldchange Pvaue Cancer
ENSG00000105568 0.57 3.45e-29 BRCA
Ensembl ID Gene symbol Cancer types Pubmed ID
ENSG00000105568 Wilms tumor 11360189
ENSG00000105568 breast cancer 19890961
ENSG00000105568 tumor 20826764
ENSG00000105568 tumours 21381030
ENSG00000105568 ovarian tumors 21435433
ENSG00000105568 tumor 21683865
ENSG00000105568 endometrial cancer 21882256
ENSG00000105568 tumours 22653804
ENSG00000105568 cancer 23359684
ENSG00000105568 tumor 23493267
ENSG00000105568 breast cancer 23555712
ENSG00000105568 ovarian cancer 23588898
ENSG00000105568 tumors 23636398
ENSG00000105568 tumor 23765252
ENSG00000105568 pancreatic cancer 23780887
ENSG00000105568 lung cancer 24204789
ENSG00000105568 tumor 24425774
ENSG00000105568 tumor 24451280
ENSG00000105568 ovarian cancer 24472300
ENSG00000105568 cancers 24671188
ENSG00000105568 tumors 25072932
ENSG00000105568 tumours 25308272
ENSG00000105568 tumor 25659743
ENSG00000105568 tumours 25867001
ENSG00000105568 tumor 26626801
ENSG00000105568 metastatic tumors 27023146
ENSG00000105568 endometrial cancer 27272709
ENSG00000105568 tumors 27348297
ENSG00000105568 tumor 27469332
ENSG00000105568 Uterine Cancer 27485451
ENSG00000105568 tumours 27499902
ENSG00000105568 uterine cancers 27556014
ENSG00000105568 tumor 27557495
ENSG00000105568 cancers 27611305
ENSG00000105568 cancer 27791010
ENSG00000105568 cancer 27847479
ENSG00000105568 lung cancer 28383694
ENSG00000105568 cancer 28489996
ENSG00000105568 Cancer 28718916
ENSG00000105568 breast cancer 28919038
ENSG00000105568 tumor 28940304
ENSG00000105568 cancer 29389895
ENSG00000105568 cancer 29444159
ENSG00000105568 laryngeal cancer 29755572
ENSG00000105568 tumor 29861864
ENSG00000105568 tumour 30104481
ENSG00000105568 cancer 30377392
ENSG00000105568 tumors 30485824
ENSG00000105568 tumor 30508944
ENSG00000105568 cancer 30787852
ENSG00000105568 cancer 31214504
ENSG00000105568 tumors 31357169
ENSG00000105568 endometrial cancer 31416848
ENSG00000105568 cancer 31541192
ENSG00000105568 tumour 31550396
ENSG00000105568 tumours 31623614
Ensembl ID Gene symbol Disease/phenotype Mutation type Mutated / Total samples Literature
ENSG00000105568 Endometrial Clear Cell Adenocarcinoma sequence_alteration 16.07% (18/112) 2 entries
ENSG00000105568 Endometrial Clear Cell Adenocarcinoma missense_variant 16.07% (18/112) 4 entries
ENSG00000105568 endometrium adenocarcinoma missense_variant 17.95% (7/39) 5 entries
ENSG00000105568 colorectal adenocarcinoma frameshift_variant 3.987% (48/1204) 2 entries
ENSG00000105568 lung carcinoma missense_variant 8.955% (12/134) 1 entry
ENSG00000105568 ovarian clear cell adenocarcinoma missense_variant 7.54% (19/252) 7 entries
ENSG00000105568 lung carcinoma sequence_alteration 8.955% (12/134) 1 entry
ENSG00000105568 Uterine Carcinosarcoma sequence_alteration 9.91% (22/222) 3 entries
ENSG00000105568 endometrial carcinoma sequence_alteration 30.14% (66/219) 6 entries
ENSG00000105568 Endometrial Endometrioid Adenocarcinoma sequence_alteration 5.516% (69/1251) 2 entries
ENSG00000105568 endometrial carcinoma missense_variant 30.14% (66/219) 7 entries
ENSG00000105568 Uterine Carcinosarcoma missense_variant 9.91% (22/222) 3 entries
ENSG00000105568 Endometrial Endometrioid Adenocarcinoma missense_variant 5.516% (69/1251) 6 entries
ENSG00000105568 colorectal adenocarcinoma sequence_alteration 3.987% (48/1204) 2 entries
ENSG00000105568 colorectal adenocarcinoma missense_variant 3.987% (48/1204) 3 entries
ENSG00000105568 prostate adenocarcinoma missense_variant 1.297% (28/2158) 3 entries
ENSG00000105568 skin melanoma missense_variant 1.105% (13/1176) 4 entries
ENSG00000105568 female breast carcinoma missense_variant 0.3745% (2/534) 1 entry
ENSG00000105568 esophageal squamous cell carcinoma sequence_alteration 1.02% (7/686) 2 entries
ENSG00000105568 Gastrointestinal stromal tumor missense_variant 1.974% (3/152) 1 entry
ENSG00000105568 Ovarian Endometrioid Adenocarcinoma missense_variant 6.471% (11/170) 4 entries
ENSG00000105568 hemangioblastoma sequence_alteration 11.43% (4/35) 1 entry
ENSG00000105568 clear cell renal carcinoma sequence_alteration 0.3219% (6/1864) 2 entries
ENSG00000105568 Vulvar Squamous Cell Carcinoma missense_variant 2.679% (3/112) 1 entry
ENSG00000105568 breast carcinoma missense_variant 0.5161% (8/1550) 3 entries
ENSG00000105568 colon adenocarcinoma sequence_alteration 2.243% (29/1293) 4 entries
ENSG00000105568 brain glioblastoma missense_variant 0.495% (6/1212) 1 entry
ENSG00000105568 breast ductal adenocarcinoma missense_variant 1.563% (25/1599) 1 entry
ENSG00000105568 prostate carcinoma sequence_alteration 0.6198% (3/484) 1 entry
ENSG00000105568 gastric adenocarcinoma sequence_alteration 1.427% (12/841) 2 entries
ENSG00000105568 esophageal adenocarcinoma sequence_alteration 2.19% (12/548) 1 entry
ENSG00000105568 Endometrial Endometrioid Adenocarcinoma conservative_inframe_deletion 5.516% (69/1251) 1 entry
ENSG00000105568 colon carcinoma missense_variant 25.0% (2/8) 1 entry
ENSG00000105568 esophageal squamous cell carcinoma missense_variant 1.02% (7/686) 3 entries
ENSG00000105568 large cell lung carcinoma missense_variant 21.05% (4/19) 3 entries
ENSG00000105568 Extramammary Paget Disease missense_variant 66.67% (2/3) 2 entries
ENSG00000105568 ovarian serous adenocarcinoma missense_variant 0.8696% (10/1150) 4 entries
ENSG00000105568 squamous cell lung carcinoma missense_variant 1.406% (14/996) 3 entries
ENSG00000105568 skin melanoma stop_gained 1.105% (13/1176) 1 entry
ENSG00000105568 colon adenocarcinoma missense_variant 2.243% (29/1293) 6 entries
ENSG00000105568 Endometrial Undifferentiated Carcinoma missense_variant 10.87% (5/46) 2 entries
ENSG00000105568 Mixed Lobular and Ductal Breast Carcinoma missense_variant 3.125% (2/64) 1 entry
ENSG00000105568 brain glioblastoma frameshift_variant 0.495% (6/1212) 1 entry
ENSG00000105568 pancreatic ductal adenocarcinoma missense_variant 1.281% (22/1718) 3 entries
ENSG00000105568 rectal adenocarcinoma missense_variant 0.9158% (5/546) 1 entry
ENSG00000105568 HER2 Positive Breast Carcinoma stop_gained 2.128% (4/188) 1 entry
ENSG00000105568 cecum adenocarcinoma missense_variant 1.852% (5/270) 2 entries
ENSG00000105568 large cell lung carcinoma sequence_alteration 21.05% (4/19) 3 entries
ENSG00000105568 skin melanoma sequence_alteration 1.105% (13/1176) 2 entries
ENSG00000105568 lung adenocarcinoma missense_variant 1.156% (30/2595) 4 entries
ENSG00000105568 breast carcinoma sequence_alteration 0.5161% (8/1550) 3 entries
ENSG00000105568 gastric adenocarcinoma missense_variant 1.427% (12/841) 2 entries
ENSG00000105568 prostate adenocarcinoma sequence_alteration 1.297% (28/2158) 2 entries
ENSG00000105568 ovarian serous adenocarcinoma sequence_alteration 0.8696% (10/1150) 2 entries
ENSG00000105568 Ovarian Endometrioid Adenocarcinoma sequence_alteration 6.471% (11/170) 2 entries
ENSG00000105568 Extramammary Paget Disease sequence_alteration 66.67% (2/3) 2 entries
ENSG00000105568 ovarian mucinous adenocarcinoma missense_variant 2.174% (2/92) 1 entry
ENSG00000105568 lung adenocarcinoma sequence_alteration 1.156% (30/2595) 2 entries
ENSG00000105568 Gallbladder Adenocarcinoma sequence_alteration 1.212% (2/165) 1 entry
ENSG00000105568 hepatocellular carcinoma missense_variant 0.8122% (8/985) 1 entry
ENSG00000105568 rectal adenocarcinoma sequence_alteration 0.9158% (5/546) 1 entry
ENSG00000105568 brain glioblastoma sequence_alteration 0.495% (6/1212) 3 entries
ENSG00000105568 Thyroid Gland Undifferentiated (Anaplastic) Carcinoma missense_variant 1.136% (3/264) 1 entry
ENSG00000105568 bladder transitional cell carcinoma missense_variant 1.728% (8/463) 1 entry
ENSG00000105568 colon adenocarcinoma frameshift_variant 2.243% (29/1293) 1 entry
ENSG00000105568 non-small cell lung carcinoma sequence_alteration 0.8772% (1/114) 1 entry
ENSG00000105568 bile duct adenocarcinoma missense_variant 0.2551% (1/392) 1 entry
ENSG00000105568 oral squamous cell carcinoma missense_variant 0.3817% (1/262) 1 entry
ENSG00000105568 Pleural Epithelioid Mesothelioma sequence_alteration 0.5% (1/200) 1 entry
ENSG00000105568 ovarian adenocarcinoma missense_variant 16.67% (1/6) 1 entry
ENSG00000105568 Appendix Adenocarcinoma missense_variant 1.351% (1/74) 1 entry
ENSG00000105568 pharyngeal squamous cell carcinoma missense_variant 1.235% (1/81) 1 entry
ENSG00000105568 hemangioblastoma missense_variant 11.43% (4/35) 1 entry
ENSG00000105568 pharyngeal squamous cell carcinoma sequence_alteration 1.235% (1/81) 1 entry
ENSG00000105568 urothelial carcinoma sequence_alteration 1.163% (1/86) 1 entry
ENSG00000105568 astrocytoma missense_variant 14.29% (1/7) 1 entry
ENSG00000105568 rectal adenocarcinoma stop_gained 0.9158% (5/546) 1 entry
ENSG00000105568 basal cell carcinoma missense_variant 1.471% (1/68) 1 entry
ENSG00000105568 small intestinal adenocarcinoma missense_variant 4.762% (1/21) 1 entry
ENSG00000105568 Bladder Adenocarcinoma missense_variant 14.29% (1/7) 1 entry
ENSG00000105568 Borderline Ovarian Surface Epithelial-Stromal Tumor missense_variant 100.0% (1/1) 1 entry
ENSG00000105568 diffuse gastric adenocarcinoma missense_variant 1.22% (1/82) 1 entry
ENSG00000105568 pancreatic neuroendocrine tumor missense_variant 2.119% (5/236) 1 entry
ENSG00000105568 Endometrial Undifferentiated Carcinoma sequence_alteration 10.87% (5/46) 1 entry
ENSG00000105568 lobular breast carcinoma missense_variant 0.4202% (1/238) 1 entry
ENSG00000105568 small cell lung carcinoma missense_variant 0.2242% (1/446) 1 entry
ENSG00000105568 Duodenal Adenocarcinoma missense_variant 5.882% (1/17) 1 entry
ENSG00000105568 urothelial carcinoma missense_variant 1.163% (1/86) 1 entry
ENSG00000105568 colon adenocarcinoma stop_gained 2.243% (29/1293) 1 entry
ENSG00000105568 esophageal adenocarcinoma missense_variant 2.19% (12/548) 1 entry
ENSG00000105568 papillary thyroid carcinoma missense_variant 0.1938% (1/516) 1 entry
ENSG00000105568 neoplasm sequence_alteration 3.448% (1/29) 1 entry
ENSG00000105568 small cell lung carcinoma sequence_alteration 0.2242% (1/446) 1 entry
ENSG00000105568 cecum adenocarcinoma sequence_alteration 1.852% (5/270) 1 entry
ENSG00000105568 breast carcinoma frameshift_variant 0.5161% (8/1550) 1 entry
ENSG00000105568 Gallbladder Adenocarcinoma missense_variant 1.212% (2/165) 1 entry
ENSG00000105568 chronic myelomonocytic leukemia missense_variant 3.704% (1/27) 1 entry
ENSG00000105568 female breast carcinoma sequence_alteration 0.3745% (2/534) 1 entry
ENSG00000105568 oral squamous cell carcinoma sequence_alteration 0.3817% (1/262) 1 entry
ENSG00000105568 basal cell carcinoma sequence_alteration 1.471% (1/68) 1 entry
ENSG00000105568 gastric intestinal type adenocarcinoma sequence_alteration 1.176% (1/85) 1 entry
ENSG00000105568 mucosal melanoma sequence_alteration 1.429% (1/70) 1 entry
ENSG00000105568 pancreatic ductal adenocarcinoma frameshift_variant 1.281% (22/1718) 1 entry
ENSG00000105568 melanoma missense_variant 0.6897% (1/145) 1 entry
ENSG00000105568 Maxillary Sinus Adenoid Cystic Carcinoma missense_variant 100.0% (1/1) 1 entry
ENSG00000105568 astrocytoma sequence_alteration 14.29% (1/7) 1 entry
ENSG00000105568 undifferentiated pleomorphic sarcoma missense_variant 1.613% (1/62) 1 entry
ENSG00000105568 breast ductal adenocarcinoma conservative_inframe_deletion 1.563% (25/1599) 1 entry
ENSG00000105568 Cervical Clear Cell Adenocarcinoma missense_variant 100.0% (1/1) 1 entry
ENSG00000105568 mucosal melanoma missense_variant 1.429% (1/70) 1 entry
ENSG00000105568 clear cell renal carcinoma frameshift_variant 0.3219% (6/1864) 1 entry
ENSG00000105568 rhabdomyosarcoma missense_variant 2.778% (1/36) 1 entry
ENSG00000105568 diffuse gastric adenocarcinoma sequence_alteration 1.22% (1/82) 1 entry
ENSG00000105568 chronic myelomonocytic leukemia sequence_alteration 3.704% (1/27) 1 entry
ENSG00000105568 Thymoma Type B3 missense_variant 8.333% (1/12) 1 entry
ENSG00000105568 Pleural Epithelioid Mesothelioma missense_variant 0.5% (1/200) 1 entry
ENSG00000105568 ovarian adenocarcinoma sequence_alteration 16.67% (1/6) 1 entry
ENSG00000105568 gastric intestinal type adenocarcinoma stop_gained 1.176% (1/85) 1 entry
ENSG00000105568 rhabdomyosarcoma sequence_alteration 2.778% (1/36) 1 entry
ENSG00000105568 non-small cell lung carcinoma missense_variant 0.8772% (1/114) 1 entry
ENSG00000105568 major salivary gland adenoid cystic carcinoma missense_variant 4.0% (1/25) 1 entry
Ensembl ID Gene symbol Cancer P-value Which worse show
ENSG00000105568 MESO 0.0087 high
ENSG00000105568 SARC 0.00044 high
ENSG00000105568 UVM 0.044 low
ENSG00000105568 PAAD 0.0049 low
ENSG00000105568 UCEC 0.049 low
ENSG00000105568 THCA 0.013 low
ENSG00000105568 ACC 0.017 high
ENSG00000105568 LUSC 0.005 high
ENSG00000105568 KIRP 0.0021 low
ENSG00000105568 KICH 0.0085 low
ENSG00000105568 LUAD 0.0032 high
ENSG00000105568 COAD 0.047 high
ENSG00000105568 ESCA 0.014 high
ENSG00000105568 TGCT 0.036 high
ENSG00000105568 BLCA 0.00036 low
ENSG00000105568 LAML 3e-04 high
ENSG00000105568 CESC 0.0041 low
ENSG00000105568 LIHC 0.00023 high
Ensembl ID Gene symbol Cancer CNV type -log10(q-value) G-score average amplitude frequency
ENSG00000105568 LUSC Del 2.748808 0.091625 0.368179 0.265469
ENSG00000105568 LUAD Del 1.833157 0.065463 0.317821 0.354651
ENSG00000105568 LGG Del 21.926120 0.160815 0.666324 0.520468
ENSG00000105568 CESC Del 0.730104 0.067528 0.427969 0.115254
ENSG00000105568 SARC Del 3.228827 0.184093 0.452457 0.326848
ENSG00000105568 GBM Del 13.061475 0.142790 0.541448 0.164645
ENSG00000105568 PAAD Del 0.903299 0.049425 0.296166 0.119565
ENSG00000105568 TGCT Del 1.064095 0.064237 0.344012 0.386667
ENSG00000105568 UCEC Del 1.042411 0.052425 0.455977 0.115028
ENSG00000105568 OV Del 12.345403 0.321429 0.567363 0.495682