Ensembl ID ENSG00000187735 Gene ID 6917 Accession 11612
Gene Symbol TCEA1 Alias SII;TCEA;TF2S;GTF2S;TFIIS Full Name transcription elongation factor A1
Position 8 : 53966552 - 54022456 Length 55905 bases Strand Minus strand
Status Confidence Main interacting RNAsN.A.RBP type Non-canonical_RBPs
Summary Predicted to enable DNA binding activity; translation elongation factor activity; and zinc ion binding activity. Predicted to be involved in positive regulation of transcription by RNA polymerase II. Predicted to act upstream of or within erythrocyte differentiation and positive regulation of transcription, DNA-templated. Located in nucleolus and nucleoplasm. Part of transcription factor TFIID complex. [provided by Alliance of Genome Resources, Apr 2022]

ENSG00000187735 Expression In 33 Tumors

Ensembl ID Gene symbol Log2 Foldchange Pvaue Cancer
ENSG00000187735 0.43 8.31e-13 BRCA
ENSG00000187735 0.69 9.65e-16 LUSC
ENSG00000187735 1.27 1.50e-13 GBM
ENSG00000187735 0.64 1.40e-14 LUAD
Ensembl ID Gene symbol Cancer types Pubmed ID
ENSG00000187735 cancer 18474089
ENSG00000187735 tumors 21596312
ENSG00000187735 mixed tumors 21927843
ENSG00000187735 ovarian cancer 23357533
ENSG00000187735 cancer 25469175
ENSG00000187735 cancer 27005522
ENSG00000187735 tumor 29741668
Ensembl ID Gene symbol Disease/phenotype Mutation type Mutated / Total samples Literature
ENSG00000187735 Salivary Gland Carcinoma ex Pleomorphic Adenoma gene_fusion 50.0% (4/8) 1 entry
ENSG00000187735 Parotid Gland Pleomorphic Adenoma gene_fusion 50.0% (3/6) 2 entries
ENSG00000187735 salivary gland adenoid cystic carcinoma gene_fusion 26.67% (36/135) 2 entries
ENSG00000187735 Salivary Gland Pleomorphic Adenoma gene_fusion 50.0% (48/96) 3 entries
ENSG00000187735 salivary gland mucoepidermoid carcinoma gene_fusion 33.33% (2/6) 1 entry
ENSG00000187735 lung adenocarcinoma sequence_alteration 0.2459% (3/1220) 1 entry
ENSG00000187735 gastric intestinal type adenocarcinoma frameshift_variant 2.353% (2/85) 1 entry
ENSG00000187735 prostate adenocarcinoma sequence_alteration 2.27% (33/1454) 2 entries
ENSG00000187735 cecum adenocarcinoma sequence_alteration 1.6% (2/125) 1 entry
ENSG00000187735 rectal adenocarcinoma missense_variant 3.167% (7/221) 1 entry
ENSG00000187735 colon adenocarcinoma missense_variant 2.909% (21/722) 4 entries
ENSG00000187735 colon adenocarcinoma sequence_alteration 2.909% (21/722) 6 entries
ENSG00000187735 Salivary Gland Basal Cell Adenocarcinoma gene_fusion 50.0% (1/2) 1 entry
ENSG00000187735 colorectal adenocarcinoma sequence_alteration 1.23% (14/1138) 2 entries
ENSG00000187735 clear cell renal carcinoma sequence_alteration 0.2177% (3/1378) 1 entry
ENSG00000187735 rectal adenocarcinoma sequence_alteration 3.167% (7/221) 1 entry
ENSG00000187735 colorectal adenocarcinoma missense_variant 1.23% (14/1138) 2 entries
ENSG00000187735 skin melanoma missense_variant 0.4137% (4/967) 1 entry
ENSG00000187735 brain glioblastoma sequence_alteration 0.324% (3/926) 1 entry
ENSG00000187735 prostate adenocarcinoma missense_variant 2.27% (33/1454) 1 entry
ENSG00000187735 bile duct adenocarcinoma missense_variant 0.5291% (1/189) 1 entry
ENSG00000187735 bronchoalveolar adenocarcinoma missense_variant 4.545% (1/22) 1 entry
ENSG00000187735 melanoma missense_variant 0.9901% (1/101) 1 entry
ENSG00000187735 lung adenocarcinoma missense_variant 0.2459% (3/1220) 1 entry
ENSG00000187735 osteosarcoma sequence_alteration 0.8621% (1/116) 1 entry
ENSG00000187735 gastric intestinal type adenocarcinoma sequence_alteration 2.353% (2/85) 1 entry
ENSG00000187735 Brain Stem Glioblastoma sequence_alteration 1.786% (1/56) 1 entry
ENSG00000187735 bronchoalveolar adenocarcinoma sequence_alteration 4.545% (1/22) 1 entry
ENSG00000187735 melanoma sequence_alteration 0.9901% (1/101) 1 entry
ENSG00000187735 T-cell acute lymphoblastic leukemia missense_variant 0.1684% (1/594) 1 entry
ENSG00000187735 squamous cell lung carcinoma sequence_alteration 0.1212% (1/825) 1 entry
ENSG00000187735 glioma sequence_alteration 0.1727% (1/579) 1 entry
Ensembl ID Gene symbol Cancer P-value Which worse show
ENSG00000187735 MESO 0.034 high
ENSG00000187735 STAD 0.00053 high
ENSG00000187735 PAAD 0.013 high
ENSG00000187735 UCEC 0.0014 high
ENSG00000187735 THCA 0.046 high
ENSG00000187735 ACC 0.0013 high
ENSG00000187735 KICH 0.0063 high
ENSG00000187735 PCPG 0.016 high
ENSG00000187735 OV 0.012 low
ENSG00000187735 KIRC 0.00062 high
ENSG00000187735 GBM 0.0052 low
ENSG00000187735 CESC 0.038 high
ENSG00000187735 LIHC 0.044 high
Ensembl ID Gene symbol Cancer CNV type -log10(q-value) G-score average amplitude frequency
ENSG00000187735 READ Amp 1.039303 0.142890 0.758096 0.569697
ENSG00000187735 UCS Amp 4.137399 0.975531 1.292945 0.660714
ENSG00000187735 TGCT Amp 3.657681 0.242131 0.586994 0.813333
ENSG00000187735 BRCA Amp 1.174796 0.155234 0.864511 0.494444
ENSG00000187735 PRAD Amp 1.071089 0.051118 0.670411 0.243902
ENSG00000187735 UCEC Amp 1.429224 0.121007 0.766648 0.335807
ENSG00000187735 UVM Amp 3.526633 0.325223 1.517112 0.600000
ENSG00000187735 OV Amp 5.755186 0.466878 0.826837 0.511226