Ensembl ID ENSG00000110367 Gene ID 1656 Accession 2747
Gene Symbol DDX6 Alias P54;RCK;HLR2;IDDILF;Rck/p54 Full Name DEAD-box helicase 6
Position 11 : 118747763 - 118791164 Length 43402 bases Strand Minus strand
Status Confidence Main interacting RNAsmRNARBP type Canonical_RBPs
Summary This gene encodes a member of the DEAD box protein family. The protein is an RNA helicase found in P-bodies and stress granules, and functions in translation suppression and mRNA degradation. It is required for microRNA-induced gene silencing. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Mar 2012]

ENSG00000110367 Expression In 33 Tumors

Ensembl ID Gene symbol Log2 Foldchange Pvaue Cancer
Ensembl ID Gene symbol Cancer types Pubmed ID
ENSG00000110367 DDX6 tumors 10319407
ENSG00000110367 DDX6 cancer 19075689
ENSG00000110367 DDX6 cancer 23932921
ENSG00000110367 DDX6 colon cancer 26144048
ENSG00000110367 DDX6 cancer 26610392
ENSG00000110367 DDX6 tumor 26783102
ENSG00000110367 DDX6 tumor 26980748
ENSG00000110367 DDX6 cancer 27679741
ENSG00000110367 DDX6 gastric cancer 28216671
ENSG00000110367 DDX6 tumor 29262563
ENSG00000110367 DDX6 gastric cancer 29314290
ENSG00000110367 DDX6 Gastric Cancer 29987267
ENSG00000110367 DDX6 Gastric Cancer 30959742
ENSG00000110367 DDX6 cancer 31167132
Ensembl ID Gene symbol Disease/phenotype Mutation type Mutated / Total samples Literature
ENSG00000110367 DDX6 prostate adenocarcinoma sequence_alteration 1.307% (19/1454) 1 entry
ENSG00000110367 DDX6 colon adenocarcinoma missense_variant 0.831% (6/722) 1 entry
ENSG00000110367 DDX6 clear cell renal carcinoma sequence_alteration 0.2903% (4/1378) 1 entry
ENSG00000110367 DDX6 Merkel cell skin cancer sequence_alteration 6.667% (2/30) 1 entry
ENSG00000110367 DDX6 melanoma sequence_alteration 2.97% (3/101) 2 entries
ENSG00000110367 DDX6 cecum adenocarcinoma sequence_alteration 4.0% (5/125) 1 entry
ENSG00000110367 DDX6 gastric adenocarcinoma missense_variant 0.5376% (3/558) 1 entry
ENSG00000110367 DDX6 lung adenocarcinoma missense_variant 0.4098% (5/1220) 2 entries
ENSG00000110367 DDX6 small cell lung carcinoma sequence_alteration 0.6192% (2/323) 1 entry
ENSG00000110367 DDX6 skin melanoma sequence_alteration 0.6205% (6/967) 1 entry
ENSG00000110367 DDX6 chronic lymphocytic leukemia missense_variant 0.3378% (3/888) 1 entry
ENSG00000110367 DDX6 brain glioblastoma missense_variant 0.8639% (8/926) 1 entry
ENSG00000110367 DDX6 diffuse large B-cell lymphoma missense_variant 0.6557% (2/305) 1 entry
ENSG00000110367 DDX6 cecum adenocarcinoma frameshift_variant 4.0% (5/125) 1 entry
ENSG00000110367 DDX6 clear cell renal carcinoma missense_variant 0.2903% (4/1378) 1 entry
ENSG00000110367 DDX6 gastric adenocarcinoma sequence_alteration 0.5376% (3/558) 1 entry
ENSG00000110367 DDX6 brain glioblastoma sequence_alteration 0.8639% (8/926) 2 entries
ENSG00000110367 DDX6 chronic lymphocytic leukemia sequence_alteration 0.3378% (3/888) 2 entries
ENSG00000110367 DDX6 skin carcinoma sequence_alteration 4.808% (5/104) 1 entry
ENSG00000110367 DDX6 colorectal adenocarcinoma missense_variant 1.494% (17/1138) 2 entries
ENSG00000110367 DDX6 hemangioblastoma sequence_alteration 12.5% (4/32) 1 entry
ENSG00000110367 DDX6 colon adenocarcinoma sequence_alteration 0.831% (6/722) 3 entries
ENSG00000110367 DDX6 colorectal adenocarcinoma sequence_alteration 1.494% (17/1138) 2 entries
ENSG00000110367 DDX6 prostate carcinoma sequence_alteration 2.273% (11/484) 2 entries
ENSG00000110367 DDX6 skin melanoma missense_variant 0.6205% (6/967) 1 entry
ENSG00000110367 DDX6 central nervous system primitive neuroectodermal neoplasm sequence_alteration 0.6757% (3/444) 1 entry
ENSG00000110367 DDX6 lung adenocarcinoma sequence_alteration 0.4098% (5/1220) 1 entry
ENSG00000110367 DDX6 colorectal adenocarcinoma frameshift_variant 1.494% (17/1138) 1 entry
ENSG00000110367 DDX6 anaplastic oligodendroglioma missense_variant 2.381% (1/42) 1 entry
ENSG00000110367 DDX6 Gallbladder Adenocarcinoma sequence_alteration 1.149% (1/87) 1 entry
ENSG00000110367 DDX6 Thyroid Gland Oncocytic Follicular Carcinoma conservative_inframe_deletion 50.0% (1/2) 1 entry
ENSG00000110367 DDX6 endometrial carcinoma sequence_alteration 4.348% (1/23) 1 entry
ENSG00000110367 DDX6 central nervous system primitive neuroectodermal neoplasm missense_variant 0.6757% (3/444) 1 entry
ENSG00000110367 DDX6 prostate adenocarcinoma missense_variant 1.307% (19/1454) 1 entry
ENSG00000110367 DDX6 cecum adenocarcinoma missense_variant 4.0% (5/125) 1 entry
ENSG00000110367 DDX6 prostate carcinoma missense_variant 2.273% (11/484) 1 entry
ENSG00000110367 DDX6 endometrial carcinoma missense_variant 4.348% (1/23) 1 entry
ENSG00000110367 DDX6 Pancreatic Acinar Cell Carcinoma sequence_alteration 5.0% (1/20) 1 entry
ENSG00000110367 DDX6 ovarian serous adenocarcinoma missense_variant 0.1486% (1/673) 1 entry
ENSG00000110367 DDX6 colorectal adenocarcinoma stop_gained 1.494% (17/1138) 1 entry
ENSG00000110367 DDX6 nasopharyngeal squamous cell carcinoma sequence_alteration 0.5988% (1/167) 1 entry
ENSG00000110367 DDX6 primary peritoneal carcinoma (disease) sequence_alteration 100.0% (1/1) 1 entry
ENSG00000110367 DDX6 nasopharyngeal squamous cell carcinoma missense_variant 0.5988% (1/167) 1 entry
ENSG00000110367 DDX6 ovarian serous adenocarcinoma sequence_alteration 0.1486% (1/673) 1 entry
ENSG00000110367 DDX6 Thyroid Gland Oncocytic Follicular Carcinoma sequence_alteration 50.0% (1/2) 1 entry
ENSG00000110367 DDX6 diffuse gastric adenocarcinoma sequence_alteration 1.266% (1/79) 1 entry
ENSG00000110367 DDX6 small cell lung carcinoma stop_gained 0.6192% (2/323) 1 entry
Ensembl ID Gene symbol Cancer P-value Which worse show
ENSG00000110367 DDX6 MESO 0.039 low
ENSG00000110367 DDX6 STAD 0.0042 low
ENSG00000110367 DDX6 CHOL 0.0099 low
ENSG00000110367 DDX6 UVM 0.027 high
ENSG00000110367 DDX6 UCEC 0.018 low
ENSG00000110367 DDX6 HNSC 0.037 low
ENSG00000110367 DDX6 READ 0.039 low
ENSG00000110367 DDX6 KICH 0.022 high
ENSG00000110367 DDX6 LUAD 0.027 low
ENSG00000110367 DDX6 PCPG 0.012 high
ENSG00000110367 DDX6 THYM 0.028 low
ENSG00000110367 DDX6 UCS 0.013 low
ENSG00000110367 DDX6 ESCA 0.014 low
ENSG00000110367 DDX6 GBM 0.034 low
ENSG00000110367 DDX6 CESC 0.044 high
ENSG00000110367 DDX6 LIHC 0.0018 high
Ensembl ID Gene symbol Cancer CNV type -log10(q-value) G-score average amplitude frequency
ENSG00000110367 DDX6 LUSC Del 2.405715 0.087952 0.349323 0.347305
ENSG00000110367 DDX6 LUAD Del 2.641751 0.073645 0.329720 0.213178
ENSG00000110367 DDX6 LGG Amp 2.319035 0.067541 0.472161 0.167641
ENSG00000110367 DDX6 CESC Del 27.435482 0.303509 0.576945 0.545763
ENSG00000110367 DDX6 KIRP Del 4.225494 0.059019 0.587185 0.104167
ENSG00000110367 DDX6 SARC Del 6.168065 0.236329 0.552309 0.466926
ENSG00000110367 DDX6 ESCA Del 1.410083 0.117091 0.435334 0.413043
ENSG00000110367 DDX6 SKCM Del 22.023136 0.252225 0.553017 0.550409
ENSG00000110367 DDX6 HNSC Del 16.501983 0.154931 0.439300 0.467433
ENSG00000110367 DDX6 LIHC Del 2.581826 0.093342 0.487324 0.251351
ENSG00000110367 DDX6 PCPG Del 0.883794 0.062152 0.614542 0.283951
ENSG00000110367 DDX6 TGCT Del 5.037471 0.140744 0.477357 0.806667
ENSG00000110367 DDX6 BLCA Del 2.812167 0.109326 0.401825 0.370098
ENSG00000110367 DDX6 BRCA Del 48.206798 0.222043 0.518318 0.492593
ENSG00000110367 DDX6 STAD Del 1.083000 0.066285 0.361275 0.199546
ENSG00000110367 DDX6 PRAD Del 1.581281 0.083399 0.496329 0.083333
ENSG00000110367 DDX6 UCEC Del 0.668176 0.047002 0.481705 0.139147
ENSG00000110367 DDX6 UVM Del 1.063142 0.071726 0.581446 0.075000