Ensembl ID ENSG00000147140 Gene ID 4841 Accession 7871
Gene Symbol NONO Alias P54;NMT55;NRB54;MRXS34;P54NRB;PPP1R114 Full Name non-POU domain containing octamer binding
Position X : 71254814 - 71301522 Length 46709 bases Strand Plus strand
Status Confidence Main interacting RNAsncRNARBP type Canonical_RBPs
Summary This gene encodes an RNA-binding protein which plays various roles in the nucleus, including transcriptional regulation and RNA splicing. A rearrangement between this gene and the transcription factor E3 gene has been observed in papillary renal cell carcinoma. Alternatively spliced transcript variants have been described. Pseudogenes exist on Chromosomes 2 and 16. [provided by RefSeq, Feb 2009]

ENSG00000147140 Expression In 33 Tumors

Ensembl ID Gene symbol Log2 Foldchange Pvaue Cancer
ENSG00000147140 NONO 0.45 9.35e-31 BRCA
ENSG00000147140 NONO 0.86 3.17e-37 COAD
ENSG00000147140 NONO 0.96 3.32e-13 READ
ENSG00000147140 NONO 0.79 4.80e-41 LUSC
ENSG00000147140 NONO 0.35 1.21e-15 PRAD
ENSG00000147140 NONO 1.11 3.31e-11 GBM
ENSG00000147140 NONO 0.62 2.07e-23 LUAD
Ensembl ID Gene symbol Cancer types Pubmed ID
ENSG00000147140 NONO breast tumors 11710964
ENSG00000147140 NONO tumour 18042045
ENSG00000147140 NONO tumor 21459849
ENSG00000147140 NONO colorectal cancer 22118625
ENSG00000147140 NONO tumors 22682314
ENSG00000147140 NONO tumor 22741017
ENSG00000147140 NONO cancer 22941645
ENSG00000147140 NONO cancer 23676460
ENSG00000147140 NONO cancer 23730526
ENSG00000147140 NONO cancer 24101161
ENSG00000147140 NONO tumor 24676409
ENSG00000147140 NONO tumours 25048860
ENSG00000147140 NONO tumour 25893301
ENSG00000147140 NONO breast cancer 26148231
ENSG00000147140 NONO Cancer 26561285
ENSG00000147140 NONO renal cancers 26975036
ENSG00000147140 NONO breast tumors 27084935
ENSG00000147140 NONO colorectal cancer 27259250
ENSG00000147140 NONO tumour 27816966
ENSG00000147140 NONO breast cancer 28334947
ENSG00000147140 NONO breast cancer 28673861
ENSG00000147140 NONO Wilms tumors 28825729
ENSG00000147140 NONO cancer 29150959
ENSG00000147140 NONO tumors 29309627
ENSG00000147140 NONO tumor 29535823
ENSG00000147140 NONO cancer 29620226
ENSG00000147140 NONO gastric cancer 29773901
ENSG00000147140 NONO tumor 29916534
ENSG00000147140 NONO cancer 30377567
ENSG00000147140 NONO triple-negative breast cancer 30725116
ENSG00000147140 NONO cancer 30767760
ENSG00000147140 NONO cancer 30824709
ENSG00000147140 NONO tumour 30946555
ENSG00000147140 NONO cancer 31189127
ENSG00000147140 NONO mesenchymal tumor 31277953
ENSG00000147140 NONO breast cancer 31733123
ENSG00000147140 NONO liver cancer 31815296
ENSG00000147140 NONO breast cancer 9360842
Ensembl ID Gene symbol Disease/phenotype Mutation type Mutated / Total samples Literature
ENSG00000147140 NONO renal carcinoma gene_fusion 18.18% (2/11) 2 entries
ENSG00000147140 NONO squamous cell lung carcinoma sequence_alteration 0.3937% (3/762) 1 entry
ENSG00000147140 NONO melanoma missense_variant 3.922% (4/102) 2 entries
ENSG00000147140 NONO kidney Wilms tumor sequence_alteration 1.736% (17/979) 1 entry
ENSG00000147140 NONO colon adenocarcinoma sequence_alteration 2.632% (19/722) 2 entries
ENSG00000147140 NONO colorectal adenocarcinoma missense_variant 1.054% (12/1138) 2 entries
ENSG00000147140 NONO cecum adenocarcinoma sequence_alteration 4.8% (6/125) 1 entry
ENSG00000147140 NONO Renal Cell Carcinoma Associated with Xp11.2 Translocations/TFE3 Gene Fusions gene_fusion 50.0% (1/2) 1 entry
ENSG00000147140 NONO skin melanoma sequence_alteration 1.758% (17/967) 1 entry
ENSG00000147140 NONO kidney Wilms tumor missense_variant 1.736% (17/979) 1 entry
ENSG00000147140 NONO breast carcinoma sequence_alteration 0.3544% (5/1411) 1 entry
ENSG00000147140 NONO skin melanoma missense_variant 1.758% (17/967) 3 entries
ENSG00000147140 NONO colorectal adenocarcinoma sequence_alteration 1.054% (12/1138) 1 entry
ENSG00000147140 NONO brain glioblastoma stop_gained 0.4315% (4/927) 1 entry
ENSG00000147140 NONO cecum adenocarcinoma missense_variant 4.8% (6/125) 1 entry
ENSG00000147140 NONO brain glioblastoma missense_variant 0.4315% (4/927) 1 entry
ENSG00000147140 NONO breast carcinoma missense_variant 0.3544% (5/1411) 1 entry
ENSG00000147140 NONO prostate adenocarcinoma sequence_alteration 0.619% (9/1454) 1 entry
ENSG00000147140 NONO lung adenocarcinoma missense_variant 0.9458% (11/1163) 3 entries
ENSG00000147140 NONO esophageal adenocarcinoma missense_variant 0.4566% (2/438) 1 entry
ENSG00000147140 NONO gastric intestinal type adenocarcinoma missense_variant 2.353% (2/85) 2 entries
ENSG00000147140 NONO ovarian serous adenocarcinoma missense_variant 0.2972% (2/673) 1 entry
ENSG00000147140 NONO colon adenocarcinoma missense_variant 2.632% (19/722) 4 entries
ENSG00000147140 NONO small cell lung carcinoma missense_variant 1.25% (4/320) 2 entries
ENSG00000147140 NONO central nervous system primitive neuroectodermal neoplasm frameshift_variant 0.885% (4/452) 1 entry
ENSG00000147140 NONO prostate carcinoma frameshift_variant 0.4695% (2/426) 1 entry
ENSG00000147140 NONO T-cell acute lymphoblastic leukemia missense_variant 0.2632% (1/380) 1 entry
ENSG00000147140 NONO clear cell renal carcinoma sequence_alteration 0.2901% (4/1379) 1 entry
ENSG00000147140 NONO myelodysplastic syndrome frameshift_variant 1.351% (1/74) 1 entry
ENSG00000147140 NONO skin melanoma frameshift_variant 1.758% (17/967) 1 entry
ENSG00000147140 NONO colon adenocarcinoma frameshift_variant 2.632% (19/722) 1 entry
ENSG00000147140 NONO esophageal adenocarcinoma sequence_alteration 0.4566% (2/438) 1 entry
ENSG00000147140 NONO esophageal squamous cell carcinoma sequence_alteration 0.1481% (1/675) 1 entry
ENSG00000147140 NONO female breast carcinoma missense_variant 0.3745% (1/267) 1 entry
ENSG00000147140 NONO colorectal adenocarcinoma stop_gained 1.054% (12/1138) 1 entry
ENSG00000147140 NONO bronchoalveolar adenocarcinoma frameshift_variant 4.545% (1/22) 1 entry
ENSG00000147140 NONO head and neck squamous cell carcinoma missense_variant 0.134% (1/746) 1 entry
ENSG00000147140 NONO cecum adenocarcinoma stop_gained 4.8% (6/125) 1 entry
ENSG00000147140 NONO Unclassified Renal Cell Carcinoma missense_variant 6.667% (1/15) 1 entry
ENSG00000147140 NONO colon adenocarcinoma stop_gained 2.632% (19/722) 1 entry
ENSG00000147140 NONO embryonal rhabdomyosarcoma missense_variant 1.266% (1/79) 1 entry
ENSG00000147140 NONO prostate carcinoma sequence_alteration 0.4695% (2/426) 1 entry
ENSG00000147140 NONO female breast carcinoma sequence_alteration 0.3745% (1/267) 1 entry
ENSG00000147140 NONO oral squamous cell carcinoma missense_variant 0.4878% (1/205) 1 entry
ENSG00000147140 NONO small intestinal neuroendocrine tumor G1 missense_variant 2.381% (1/42) 1 entry
ENSG00000147140 NONO diffuse gastric adenocarcinoma sequence_alteration 1.266% (1/79) 1 entry
ENSG00000147140 NONO angiosarcoma sequence_alteration 7.143% (1/14) 1 entry
ENSG00000147140 NONO melanoma sequence_alteration 3.922% (4/102) 1 entry
ENSG00000147140 NONO Central Nervous System Lymphoma missense_variant 11.11% (1/9) 1 entry
ENSG00000147140 NONO Gallbladder Adenocarcinoma missense_variant 1.149% (1/87) 1 entry
ENSG00000147140 NONO parathyroid adenoma missense_variant 6.25% (1/16) 1 entry
ENSG00000147140 NONO melanoma stop_gained 3.922% (4/102) 1 entry
ENSG00000147140 NONO prostate carcinoma conservative_inframe_deletion 0.4695% (2/426) 1 entry
Ensembl ID Gene symbol Cancer P-value Which worse show
ENSG00000147140 NONO MESO 0.0058 high
ENSG00000147140 NONO SARC 0.00058 high
ENSG00000147140 NONO STAD 0.043 low
ENSG00000147140 NONO CHOL 0.0059 high
ENSG00000147140 NONO THCA 0.024 low
ENSG00000147140 NONO LGG 0.0045 low
ENSG00000147140 NONO LUSC 0.017 low
ENSG00000147140 NONO HNSC 0.042 high
ENSG00000147140 NONO PCPG 0.015 high
ENSG00000147140 NONO THYM 0.0012 low
ENSG00000147140 NONO BRCA 0.0061 high
ENSG00000147140 NONO ESCA 0.0011 high
ENSG00000147140 NONO OV 0.014 low
ENSG00000147140 NONO DLBC 0.046 low
ENSG00000147140 NONO TGCT 0.0072 low
ENSG00000147140 NONO BLCA 0.017 low
ENSG00000147140 NONO LAML 0.029 low
ENSG00000147140 NONO CESC 0.024 low
ENSG00000147140 NONO LIHC 0.003 high
Ensembl ID Gene symbol Cancer CNV type -log10(q-value) G-score average amplitude frequency