ENSG00000198604 Expression In 33 Tumors

Ensembl ID Gene symbol Log2 Foldchange Pvaue Cancer
ENSG00000198604 1.18 4.74e-62 KIRC
ENSG00000198604 0.55 4.84e-21 BRCA
ENSG00000198604 1.82 5.62e-13 GBM
ENSG00000198604 1.09 3.16e-24 KIRP
ENSG00000198604 0.85 4.28e-14 UCEC
Ensembl ID Gene symbol Cancer types Pubmed ID
ENSG00000198604 tumor 24244200
ENSG00000198604 tumour 29089486
ENSG00000198604 tumors 30952871
ENSG00000198604 cancer 31085244
ENSG00000198604 tumors 6976325
Ensembl ID Gene symbol Disease/phenotype Mutation type Mutated / Total samples Literature
ENSG00000198604 colorectal adenocarcinoma missense_variant 3.954% (45/1138) 2 entries
ENSG00000198604 colon adenocarcinoma stop_gained 2.165% (16/739) 1 entry
ENSG00000198604 non-small cell lung carcinoma missense_variant 3.774% (2/53) 1 entry
ENSG00000198604 ovarian serous adenocarcinoma missense_variant 0.2972% (2/673) 1 entry
ENSG00000198604 skin melanoma stop_gained 2.378% (23/967) 2 entries
ENSG00000198604 Cervical Small Cell Carcinoma missense_variant 50.0% (3/6) 1 entry
ENSG00000198604 female breast carcinoma missense_variant 1.498% (4/267) 2 entries
ENSG00000198604 T-cell acute lymphoblastic leukemia frameshift_variant 1.053% (4/380) 1 entry
ENSG00000198604 brain glioblastoma sequence_alteration 0.54% (5/926) 2 entries
ENSG00000198604 Breast Carcinoma by Gene Expression Profile missense_variant 10.53% (2/19) 1 entry
ENSG00000198604 small cell lung carcinoma missense_variant 1.258% (4/318) 1 entry
ENSG00000198604 bronchoalveolar adenocarcinoma missense_variant 9.091% (2/22) 1 entry
ENSG00000198604 diffuse large B-cell lymphoma missense_variant 0.6601% (2/303) 1 entry
ENSG00000198604 colorectal adenocarcinoma sequence_alteration 3.954% (45/1138) 1 entry
ENSG00000198604 colorectal adenocarcinoma frameshift_variant 3.954% (45/1138) 2 entries
ENSG00000198604 colon adenocarcinoma missense_variant 2.165% (16/739) 3 entries
ENSG00000198604 head and neck squamous cell carcinoma missense_variant 0.639% (4/626) 1 entry
ENSG00000198604 melanoma missense_variant 3.96% (4/101) 2 entries
ENSG00000198604 basal cell carcinoma missense_variant 8.621% (5/58) 1 entry
ENSG00000198604 prostate adenocarcinoma missense_variant 3.095% (45/1454) 1 entry
ENSG00000198604 lung adenocarcinoma missense_variant 1.376% (16/1163) 4 entries
ENSG00000198604 skin melanoma missense_variant 2.378% (23/967) 3 entries
ENSG00000198604 squamous cell lung carcinoma missense_variant 1.575% (12/762) 1 entry
ENSG00000198604 bladder transitional cell carcinoma missense_variant 2.19% (3/137) 2 entries
ENSG00000198604 prostate adenocarcinoma sequence_alteration 3.095% (45/1454) 1 entry
ENSG00000198604 bile duct adenocarcinoma missense_variant 1.058% (2/189) 1 entry
ENSG00000198604 esophageal squamous cell carcinoma missense_variant 1.923% (13/676) 5 entries
ENSG00000198604 diffuse gastric adenocarcinoma sequence_alteration 2.532% (2/79) 1 entry
ENSG00000198604 cecum adenocarcinoma missense_variant 4.762% (6/126) 2 entries
ENSG00000198604 prostate carcinoma frameshift_variant 2.582% (11/426) 1 entry
ENSG00000198604 small cell lung carcinoma frameshift_variant 1.258% (4/318) 1 entry
ENSG00000198604 esophageal squamous cell carcinoma sequence_alteration 1.923% (13/676) 1 entry
ENSG00000198604 Cervical Small Cell Carcinoma sequence_alteration 50.0% (3/6) 1 entry
ENSG00000198604 small cell lung carcinoma sequence_alteration 1.258% (4/318) 1 entry
ENSG00000198604 skin carcinoma missense_variant 7.692% (8/104) 1 entry
ENSG00000198604 brain glioblastoma frameshift_variant 0.54% (5/926) 1 entry
ENSG00000198604 nasopharyngeal squamous cell carcinoma missense_variant 0.5988% (1/167) 1 entry
ENSG00000198604 clear cell renal carcinoma sequence_alteration 0.155% (2/1290) 1 entry
ENSG00000198604 T-cell acute lymphoblastic leukemia missense_variant 1.053% (4/380) 1 entry
ENSG00000198604 T-cell acute lymphoblastic leukemia sequence_alteration 1.053% (4/380) 1 entry
ENSG00000198604 esophageal squamous cell carcinoma frameshift_variant 1.923% (13/676) 1 entry
ENSG00000198604 Fallopian Tube Serous Adenocarcinoma missense_variant 50.0% (1/2) 1 entry
ENSG00000198604 melanoma frameshift_variant 3.96% (4/101) 1 entry
ENSG00000198604 Fallopian Tube Serous Adenocarcinoma sequence_alteration 50.0% (1/2) 1 entry
ENSG00000198604 Brain Stem Glioblastoma sequence_alteration 1.786% (1/56) 1 entry
ENSG00000198604 colon carcinoma missense_variant 12.5% (1/8) 1 entry
ENSG00000198604 squamous cell lung carcinoma sequence_alteration 1.575% (12/762) 1 entry
ENSG00000198604 oral squamous cell carcinoma frameshift_variant 0.4854% (1/206) 1 entry
ENSG00000198604 colorectal adenocarcinoma stop_gained 3.954% (45/1138) 1 entry
ENSG00000198604 colon adenocarcinoma sequence_alteration 2.165% (16/739) 1 entry
ENSG00000198604 breast ductal adenocarcinoma frameshift_variant 8.266% (51/617) 1 entry
ENSG00000198604 gastric intestinal type adenocarcinoma stop_gained 1.176% (1/85) 1 entry
ENSG00000198604 Ampulla of Vater Carcinoma missense_variant 1.176% (1/85) 1 entry
ENSG00000198604 pancreatic ductal adenocarcinoma missense_variant 2.859% (36/1259) 1 entry
Ensembl ID Gene symbol Cancer P-value Which worse show
ENSG00000198604 MESO 0.012 high
ENSG00000198604 SARC 0.00012 high
ENSG00000198604 CHOL 0.037 low
ENSG00000198604 UVM 0.00048 high
ENSG00000198604 PAAD 0.0011 high
ENSG00000198604 UCEC 0.022 low
ENSG00000198604 THCA 0.041 low
ENSG00000198604 ACC 0.0089 high
ENSG00000198604 LGG 0.00018 high
ENSG00000198604 LUSC 0.037 low
ENSG00000198604 HNSC 0.016 high
ENSG00000198604 LUAD 0.037 high
ENSG00000198604 PCPG 0.0098 low
ENSG00000198604 COAD 0.042 low
ENSG00000198604 UCS 0.031 low
ENSG00000198604 OV 0.017 low
ENSG00000198604 KIRC 0.00093 high
ENSG00000198604 PRAD 0.0083 high
ENSG00000198604 BLCA 0.00026 high
ENSG00000198604 GBM 0.0052 low
ENSG00000198604 SKCM 0.00011 low
ENSG00000198604 LIHC 5e-04 high
Ensembl ID Gene symbol Cancer CNV type -log10(q-value) G-score average amplitude frequency
ENSG00000198604 LUAD Amp 39.027419 0.580154 0.795387 0.422481
ENSG00000198604 GBM Del 3.652223 0.081996 0.600811 0.292894
ENSG00000198604 BRCA Amp 1.174796 0.155248 0.576202 0.200000