ENSG00000169925 Expression In 33 Tumors

Ensembl ID Gene symbol Log2 Foldchange Pvaue Cancer
ENSG00000169925 -0.4 3.49e-14 KIRC
Ensembl ID Gene symbol Cancer types Pubmed ID
ENSG00000169925 bladder cancer 16008511
ENSG00000169925 tumor 20053927
ENSG00000169925 tumors 20951314
ENSG00000169925 breast cancer 24874954
ENSG00000169925 cancer 25314271
ENSG00000169925 tumour 25467295
ENSG00000169925 cancer 25849938
ENSG00000169925 cancer 26035625
ENSG00000169925 cancers 26080064
ENSG00000169925 ovarian cancer 26877780
ENSG00000169925 tumor 27169995
ENSG00000169925 squamous cell cancer 27451123
ENSG00000169925 tumors 27769352
ENSG00000169925 breast cancer 27911230
ENSG00000169925 TGCT 28026145
ENSG00000169925 primary cancer 28194432
ENSG00000169925 tumors 28339196
ENSG00000169925 cancer 28786345
ENSG00000169925 prostate cancer 28805820
ENSG00000169925 endometrial cancer 28805821
ENSG00000169925 tumors 28805822
ENSG00000169925 triple-negative breast cancer 29437854
ENSG00000169925 breast cancer 29493812
ENSG00000169925 tumor 29540837
ENSG00000169925 brain cancers 29764999
ENSG00000169925 Cancer 29961174
ENSG00000169925 cancer 30080437
ENSG00000169925 cancer 30554943
ENSG00000169925 tumors 31118674
ENSG00000169925 breast cancers 31551256
ENSG00000169925 tumor 31653826
ENSG00000169925 tumors 31767403
ENSG00000169925 cancer 31969702
Ensembl ID Gene symbol Disease/phenotype Mutation type Mutated / Total samples Literature
ENSG00000169925 colorectal adenocarcinoma frameshift_variant 4.623% (54/1168) 2 entries
ENSG00000169925 NUT midline carcinoma gene_fusion 50.0% (3/6) 2 entries
ENSG00000169925 colorectal adenocarcinoma missense_variant 4.623% (54/1168) 2 entries
ENSG00000169925 colorectal adenocarcinoma sequence_alteration 4.623% (54/1168) 1 entry
ENSG00000169925 lung adenocarcinoma missense_variant 0.6843% (8/1169) 3 entries
ENSG00000169925 esophageal squamous cell carcinoma sequence_alteration 1.037% (7/675) 2 entries
ENSG00000169925 HER2 Positive Breast Carcinoma sequence_alteration 1.515% (2/132) 1 entry
ENSG00000169925 breast carcinoma sequence_alteration 0.4961% (7/1411) 1 entry
ENSG00000169925 hairy cell leukemia sequence_alteration 9.524% (2/21) 1 entry
ENSG00000169925 colon adenocarcinoma missense_variant 2.39% (18/753) 4 entries
ENSG00000169925 lung adenocarcinoma sequence_alteration 0.6843% (8/1169) 1 entry
ENSG00000169925 melanoma missense_variant 1.98% (2/101) 1 entry
ENSG00000169925 colon adenocarcinoma frameshift_variant 2.39% (18/753) 2 entries
ENSG00000169925 esophageal adenocarcinoma missense_variant 1.826% (8/438) 1 entry
ENSG00000169925 prostate adenocarcinoma sequence_alteration 2.201% (32/1454) 1 entry
ENSG00000169925 female breast carcinoma missense_variant 1.124% (3/267) 1 entry
ENSG00000169925 clear cell renal carcinoma missense_variant 0.2257% (3/1329) 2 entries
ENSG00000169925 skin melanoma missense_variant 2.068% (20/967) 4 entries
ENSG00000169925 cecum adenocarcinoma frameshift_variant 5.344% (7/131) 1 entry
ENSG00000169925 esophageal squamous cell carcinoma missense_variant 1.037% (7/675) 2 entries
ENSG00000169925 esophageal adenocarcinoma sequence_alteration 1.826% (8/438) 1 entry
ENSG00000169925 brain glioblastoma sequence_alteration 0.432% (4/926) 1 entry
ENSG00000169925 hairy cell leukemia missense_variant 9.524% (2/21) 1 entry
ENSG00000169925 small cell lung carcinoma missense_variant 1.262% (4/317) 2 entries
ENSG00000169925 prostate adenocarcinoma missense_variant 2.201% (32/1454) 1 entry
ENSG00000169925 gastric adenocarcinoma missense_variant 2.03% (15/739) 1 entry
ENSG00000169925 lung adenocarcinoma stop_gained 0.6843% (8/1169) 2 entries
ENSG00000169925 oral squamous cell carcinoma missense_variant 1.456% (3/206) 3 entries
ENSG00000169925 colon adenocarcinoma sequence_alteration 2.39% (18/753) 2 entries
ENSG00000169925 female breast carcinoma sequence_alteration 1.124% (3/267) 1 entry
ENSG00000169925 breast carcinoma missense_variant 0.4961% (7/1411) 1 entry
ENSG00000169925 hepatocellular carcinoma missense_variant 0.7769% (7/901) 1 entry
ENSG00000169925 gastric intestinal type adenocarcinoma frameshift_variant 4.706% (4/85) 2 entries
ENSG00000169925 gastric intestinal type adenocarcinoma missense_variant 4.706% (4/85) 1 entry
ENSG00000169925 Uterine Carcinosarcoma missense_variant 2.727% (3/110) 1 entry
ENSG00000169925 nasopharyngeal squamous cell carcinoma conservative_inframe_deletion 0.5988% (1/167) 1 entry
ENSG00000169925 chronic myelomonocytic leukemia sequence_alteration 1.053% (1/95) 1 entry
ENSG00000169925 diffuse gastric adenocarcinoma sequence_alteration 1.266% (1/79) 1 entry
ENSG00000169925 adenosquamous lung carcinoma sequence_alteration 9.091% (1/11) 1 entry
ENSG00000169925 adenosquamous lung carcinoma missense_variant 9.091% (1/11) 1 entry
ENSG00000169925 small cell lung carcinoma sequence_alteration 1.262% (4/317) 1 entry
ENSG00000169925 Endometrial Endometrioid Adenocarcinoma frameshift_variant 1.996% (11/551) 1 entry
ENSG00000169925 colon adenocarcinoma conservative_inframe_deletion 2.39% (18/753) 1 entry
ENSG00000169925 Parotid Gland Adenoid Cystic Carcinoma missense_variant 11.11% (1/9) 1 entry
ENSG00000169925 skin melanoma stop_gained 2.068% (20/967) 1 entry
ENSG00000169925 basal cell carcinoma missense_variant 3.448% (2/58) 1 entry
ENSG00000169925 colon carcinoma missense_variant 12.5% (1/8) 1 entry
ENSG00000169925 Brain Stem Glioblastoma sequence_alteration 1.786% (1/56) 1 entry
ENSG00000169925 diffuse large B-cell lymphoma missense_variant 0.3289% (1/304) 1 entry
ENSG00000169925 ovarian serous adenocarcinoma missense_variant 0.1443% (1/693) 1 entry
ENSG00000169925 gastric intestinal type adenocarcinoma sequence_alteration 4.706% (4/85) 1 entry
ENSG00000169925 HER2 Positive Breast Carcinoma missense_variant 1.515% (2/132) 1 entry
ENSG00000169925 bladder transitional cell carcinoma missense_variant 0.7299% (1/137) 1 entry
ENSG00000169925 basal cell carcinoma sequence_alteration 3.448% (2/58) 1 entry
Ensembl ID Gene symbol Cancer P-value Which worse show
ENSG00000169925 SARC 0.025 high
ENSG00000169925 UVM 6e-04 low
ENSG00000169925 PAAD 0.042 low
ENSG00000169925 THCA 0.021 high
ENSG00000169925 ACC 0.00033 high
ENSG00000169925 LUSC 0.01 high
ENSG00000169925 HNSC 0.024 low
ENSG00000169925 READ 0.0069 low
ENSG00000169925 KICH 0.00081 low
ENSG00000169925 BRCA 0.049 high
ENSG00000169925 OV 0.011 high
ENSG00000169925 LAML 0.033 low
ENSG00000169925 GBM 0.022 low
ENSG00000169925 SKCM 0.026 high
ENSG00000169925 LIHC 0.0075 high
Ensembl ID Gene symbol Cancer CNV type -log10(q-value) G-score average amplitude frequency
ENSG00000169925 SARC Del 1.837877 0.153340 0.539790 0.233463
ENSG00000169925 TGCT Del 0.728347 0.056298 0.358656 0.393333
ENSG00000169925 BRCA Del 0.659616 0.062854 0.377218 0.273148
ENSG00000169925 UCEC Del 1.445192 0.057447 0.540081 0.243043
ENSG00000169925 OV Del 5.132423 0.248318 0.570737 0.588946