Ensembl ID ENSG00000047410 Gene ID 7175 Accession 12017
Gene Symbol TPR Alias MRT79 Full Name translocated promoter region, nuclear basket protein
Position 1 : 186311652 - 186375693 Length 64042 bases Strand Minus strand
Status Confidence Main interacting RNAsmRNARBP type Non-canonical_RBPs
Summary This gene encodes a large coiled-coil protein that forms intranuclear filaments attached to the inner surface of nuclear pore complexes (NPCs). The protein directly interacts with several components of the NPC. It is required for the nuclear export of mRNAs and some proteins. Oncogenic fusions of the 5' end of this gene with several different kinase genes occur in some neoplasias. [provided by RefSeq, Jul 2008]

ENSG00000047410 Expression In 33 Tumors

Ensembl ID Gene symbol Log2 Foldchange Pvaue Cancer
ENSG00000047410 TPR 0.63 3.31e-13 LIHC
Ensembl ID Gene symbol Cancer types Pubmed ID
ENSG00000047410 TPR tumor 10074915
ENSG00000047410 TPR cancer 10435641
ENSG00000047410 TPR tumor 10760755
ENSG00000047410 TPR cancer 11914137
ENSG00000047410 TPR breast cancer 15150556
ENSG00000047410 TPR tumor 18553959
ENSG00000047410 TPR breast cancer 18587674
ENSG00000047410 TPR tumor 18701492
ENSG00000047410 TPR tumors 18845790
ENSG00000047410 TPR cancer 19640296
ENSG00000047410 TPR tumor 19819693
ENSG00000047410 TPR tumor 20093405
ENSG00000047410 TPR cancer 2052572
ENSG00000047410 TPR cancer 21235734
ENSG00000047410 TPR tumor 21405128
ENSG00000047410 TPR tumor 21457491
ENSG00000047410 TPR acute myeloid leukemia (AML) 22425524
ENSG00000047410 TPR tumor 22581753
ENSG00000047410 TPR thyroid cancer 22887574
ENSG00000047410 TPR cancer 22913813
ENSG00000047410 TPR tumor 2300559
ENSG00000047410 TPR breast cancer 23075381
ENSG00000047410 TPR acute myeloid leukemia (AML) 23559008
ENSG00000047410 TPR cancer 23740762
ENSG00000047410 TPR kidney cancer 23925944
ENSG00000047410 TPR tumor 23993328
ENSG00000047410 TPR tumor 24736082
ENSG00000047410 TPR tumors 24959084
ENSG00000047410 TPR tumor 24974147
ENSG00000047410 TPR breast cancer 25159299
ENSG00000047410 TPR cancers 25471943
ENSG00000047410 TPR renal cancer 25512285
ENSG00000047410 TPR tumors 25602801
ENSG00000047410 TPR colon cancer 25925381
ENSG00000047410 TPR prostate cancer 25986567
ENSG00000047410 TPR cancer 26001971
ENSG00000047410 TPR cancers 26210452
ENSG00000047410 TPR tumors 26384300
ENSG00000047410 TPR tumors 26784937
ENSG00000047410 TPR cancers 26828588
ENSG00000047410 TPR neural tumors 27259011
ENSG00000047410 TPR GBM 27661120
ENSG00000047410 TPR cancer 28686671
ENSG00000047410 TPR tumors 29162841
ENSG00000047410 TPR breast cancer 29190905
ENSG00000047410 TPR cancer 29293508
ENSG00000047410 TPR cancers 29351209
ENSG00000047410 TPR cancer 29416781
ENSG00000047410 TPR Colorectal cancer 29568361
ENSG00000047410 TPR Tumor 29707134
ENSG00000047410 TPR tumor 30248654
ENSG00000047410 TPR cancer 30587991
ENSG00000047410 TPR tumour 30624546
ENSG00000047410 TPR tumor 31215992
ENSG00000047410 TPR gastric cancer 31279156
ENSG00000047410 TPR Tumor 31438847
ENSG00000047410 TPR tumour 6485821
ENSG00000047410 TPR tumour 7197111
ENSG00000047410 TPR gastric tumors 8289471
ENSG00000047410 TPR thyroid tumors 9172002
Ensembl ID Gene symbol Disease/phenotype Mutation type Mutated / Total samples Literature
ENSG00000047410 TPR Thyroid Gland Oncocytic Follicular Carcinoma gene_fusion 47.62% (20/42) 2 entries
ENSG00000047410 TPR Follicular Variant Thyroid Gland Papillary Carcinoma gene_fusion 50.0% (14/28) 2 entries
ENSG00000047410 TPR Benign Thyroid Gland Neoplasm gene_fusion 50.0% (65/130) 3 entries
ENSG00000047410 TPR papillary thyroid carcinoma gene_fusion 49.87% (378/758) 9 entries
ENSG00000047410 TPR follicular thyroid carcinoma gene_fusion 37.5% (6/16) 3 entries
ENSG00000047410 TPR medullary thyroid gland carcinoma gene_fusion 12.0% (3/25) 1 entry
ENSG00000047410 TPR basal cell carcinoma missense_variant 6.897% (4/58) 1 entry
ENSG00000047410 TPR anaplastic oligodendroglioma missense_variant 4.762% (2/42) 1 entry
ENSG00000047410 TPR female breast carcinoma missense_variant 2.247% (6/267) 2 entries
ENSG00000047410 TPR rectal adenocarcinoma missense_variant 6.335% (14/221) 2 entries
ENSG00000047410 TPR lung adenocarcinoma gene_fusion 3.519% (41/1165) 1 entry
ENSG00000047410 TPR nasopharyngeal squamous cell carcinoma stop_gained 2.381% (4/168) 1 entry
ENSG00000047410 TPR lung adenocarcinoma missense_variant 3.519% (41/1165) 3 entries
ENSG00000047410 TPR prostate adenocarcinoma missense_variant 3.508% (51/1454) 3 entries
ENSG00000047410 TPR Poorly Differentiated Thyroid Gland Carcinoma gene_fusion 50.0% (1/2) 1 entry
ENSG00000047410 TPR colorectal adenocarcinoma missense_variant 7.199% (82/1139) 3 entries
ENSG00000047410 TPR skin melanoma missense_variant 2.896% (28/967) 3 entries
ENSG00000047410 TPR small cell lung carcinoma missense_variant 3.448% (11/319) 3 entries
ENSG00000047410 TPR diffuse large B-cell lymphoma sequence_alteration 0.6601% (2/303) 1 entry
ENSG00000047410 TPR colon adenocarcinoma stop_gained 8.234% (62/753) 2 entries
ENSG00000047410 TPR gastric adenocarcinoma sequence_alteration 3.387% (23/679) 1 entry
ENSG00000047410 TPR oral squamous cell carcinoma missense_variant 0.9709% (2/206) 1 entry
ENSG00000047410 TPR breast ductal adenocarcinoma sequence_alteration 5.993% (35/584) 1 entry
ENSG00000047410 TPR squamous cell lung carcinoma missense_variant 4.462% (34/762) 4 entries
ENSG00000047410 TPR prostate adenocarcinoma sequence_alteration 3.508% (51/1454) 2 entries
ENSG00000047410 TPR skin melanoma sequence_alteration 2.896% (28/967) 3 entries
ENSG00000047410 TPR clear cell renal carcinoma missense_variant 0.7977% (11/1379) 1 entry
ENSG00000047410 TPR colon adenocarcinoma frameshift_variant 8.234% (62/753) 3 entries
ENSG00000047410 TPR central nervous system primitive neuroectodermal neoplasm missense_variant 1.549% (7/452) 3 entries
ENSG00000047410 TPR lung adenocarcinoma sequence_alteration 3.519% (41/1165) 4 entries
ENSG00000047410 TPR prostate carcinoma missense_variant 1.166% (5/429) 2 entries
ENSG00000047410 TPR colorectal adenocarcinoma sequence_alteration 7.199% (82/1139) 2 entries
ENSG00000047410 TPR esophageal squamous cell carcinoma sequence_alteration 2.802% (19/678) 3 entries
ENSG00000047410 TPR squamous cell lung carcinoma stop_gained 4.462% (34/762) 2 entries
ENSG00000047410 TPR colon adenocarcinoma missense_variant 8.234% (62/753) 7 entries
ENSG00000047410 TPR esophageal adenocarcinoma sequence_alteration 3.653% (16/438) 1 entry
ENSG00000047410 TPR skin melanoma stop_gained 2.896% (28/967) 1 entry
ENSG00000047410 TPR esophageal adenocarcinoma missense_variant 3.653% (16/438) 1 entry
ENSG00000047410 TPR small cell lung carcinoma stop_gained 3.448% (11/319) 2 entries
ENSG00000047410 TPR gastric intestinal type adenocarcinoma missense_variant 7.059% (6/85) 2 entries
ENSG00000047410 TPR colorectal adenocarcinoma stop_gained 7.199% (82/1139) 2 entries
ENSG00000047410 TPR clear cell renal carcinoma sequence_alteration 0.7977% (11/1379) 1 entry
ENSG00000047410 TPR hepatocellular carcinoma sequence_alteration 1.996% (18/902) 2 entries
ENSG00000047410 TPR colorectal adenocarcinoma frameshift_variant 7.199% (82/1139) 1 entry
ENSG00000047410 TPR central nervous system primitive neuroectodermal neoplasm sequence_alteration 1.549% (7/452) 1 entry
ENSG00000047410 TPR rectal adenocarcinoma sequence_alteration 6.335% (14/221) 1 entry
ENSG00000047410 TPR Ampulla of Vater Carcinoma missense_variant 2.353% (2/85) 1 entry
ENSG00000047410 TPR chronic lymphocytic leukemia sequence_alteration 1.014% (9/888) 1 entry
ENSG00000047410 TPR breast ductal adenocarcinoma missense_variant 5.993% (35/584) 1 entry
ENSG00000047410 TPR esophageal squamous cell carcinoma stop_gained 2.802% (19/678) 2 entries
ENSG00000047410 TPR brain glioblastoma sequence_alteration 0.3236% (3/927) 2 entries
ENSG00000047410 TPR melanoma missense_variant 3.922% (4/102) 1 entry
ENSG00000047410 TPR nasopharyngeal squamous cell carcinoma missense_variant 2.381% (4/168) 1 entry
ENSG00000047410 TPR cecum adenocarcinoma sequence_alteration 16.03% (21/131) 2 entries
ENSG00000047410 TPR prostate carcinoma sequence_alteration 1.166% (5/429) 1 entry
ENSG00000047410 TPR esophageal squamous cell carcinoma missense_variant 2.802% (19/678) 3 entries
ENSG00000047410 TPR pancreatic ductal adenocarcinoma missense_variant 2.621% (33/1259) 2 entries
ENSG00000047410 TPR hepatocellular carcinoma missense_variant 1.996% (18/902) 1 entry
ENSG00000047410 TPR gastric intestinal type adenocarcinoma stop_gained 7.059% (6/85) 1 entry
ENSG00000047410 TPR breast carcinoma missense_variant 1.772% (25/1411) 2 entries
ENSG00000047410 TPR colon adenocarcinoma sequence_alteration 8.234% (62/753) 3 entries
ENSG00000047410 TPR lung adenocarcinoma stop_gained 3.519% (41/1165) 1 entry
ENSG00000047410 TPR cecum adenocarcinoma missense_variant 16.03% (21/131) 2 entries
ENSG00000047410 TPR gastric adenocarcinoma missense_variant 3.387% (23/679) 2 entries
ENSG00000047410 TPR rectal adenocarcinoma stop_gained 6.335% (14/221) 1 entry
ENSG00000047410 TPR Pleural Mesothelioma missense_variant 1.031% (1/97) 1 entry
ENSG00000047410 TPR prostate adenocarcinoma frameshift_variant 3.508% (51/1454) 1 entry
ENSG00000047410 TPR meningioma (disease) missense_variant 2.041% (1/49) 1 entry
ENSG00000047410 TPR Thyroid Gland Undifferentiated (Anaplastic) Carcinoma sequence_alteration 16.67% (1/6) 1 entry
ENSG00000047410 TPR papillary renal cell carcinoma missense_variant 0.5634% (2/355) 1 entry
ENSG00000047410 TPR small cell lung carcinoma sequence_alteration 3.448% (11/319) 1 entry
ENSG00000047410 TPR hepatocellular carcinoma frameshift_variant 1.996% (18/902) 1 entry
ENSG00000047410 TPR rectal adenocarcinoma frameshift_variant 6.335% (14/221) 1 entry
ENSG00000047410 TPR Parathyroid Gland Carcinoma missense_variant 5.263% (1/19) 1 entry
ENSG00000047410 TPR basal cell carcinoma sequence_alteration 6.897% (4/58) 1 entry
ENSG00000047410 TPR acute lymphoblastic leukemia missense_variant 0.3115% (1/321) 1 entry
ENSG00000047410 TPR adenosquamous lung carcinoma sequence_alteration 9.091% (1/11) 1 entry
ENSG00000047410 TPR ovarian serous adenocarcinoma stop_gained 0.1486% (1/673) 1 entry
ENSG00000047410 TPR melanoma stop_gained 3.922% (4/102) 1 entry
ENSG00000047410 TPR pancreatic neuroendocrine tumor missense_variant 2.5% (4/160) 1 entry
ENSG00000047410 TPR mucosal melanoma sequence_alteration 7.143% (1/14) 1 entry
ENSG00000047410 TPR gastric intestinal type adenocarcinoma frameshift_variant 7.059% (6/85) 1 entry
ENSG00000047410 TPR osteosarcoma stop_gained 0.8475% (1/118) 1 entry
ENSG00000047410 TPR hepatocellular carcinoma stop_gained 1.996% (18/902) 1 entry
ENSG00000047410 TPR colon adenoma missense_variant 5.882% (1/17) 1 entry
ENSG00000047410 TPR Merkel cell skin cancer sequence_alteration 6.667% (2/30) 1 entry
ENSG00000047410 TPR non-small cell lung carcinoma sequence_alteration 5.66% (3/53) 1 entry
ENSG00000047410 TPR rectal adenocarcinoma conservative_inframe_deletion 6.335% (14/221) 1 entry
ENSG00000047410 TPR Mantle cell lymphoma sequence_alteration 2.439% (1/41) 1 entry
ENSG00000047410 TPR Extraskeletal Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor missense_variant 3.704% (1/27) 1 entry
ENSG00000047410 TPR Gallbladder Adenocarcinoma missense_variant 1.149% (1/87) 1 entry
ENSG00000047410 TPR bladder transitional cell carcinoma missense_variant 0.7299% (1/137) 1 entry
ENSG00000047410 TPR basal cell carcinoma stop_gained 6.897% (4/58) 1 entry
ENSG00000047410 TPR diffuse gastric adenocarcinoma sequence_alteration 1.266% (1/79) 1 entry
ENSG00000047410 TPR T-cell acute lymphoblastic leukemia sequence_alteration 0.2632% (1/380) 1 entry
ENSG00000047410 TPR colonic neoplasm sequence_alteration 6.667% (1/15) 1 entry
ENSG00000047410 TPR Brain Stem Glioblastoma sequence_alteration 1.786% (1/56) 1 entry
ENSG00000047410 TPR bile duct adenocarcinoma missense_variant 0.5291% (1/189) 1 entry
ENSG00000047410 TPR Merkel cell skin cancer missense_variant 6.667% (2/30) 1 entry
Ensembl ID Gene symbol Cancer P-value Which worse show
ENSG00000047410 TPR MESO 0.014 high
ENSG00000047410 TPR UVM 0.0061 high
ENSG00000047410 TPR PAAD 0.017 high
ENSG00000047410 TPR UCEC 0.048 low
ENSG00000047410 TPR THCA 0.048 high
ENSG00000047410 TPR LGG 0.00063 high
ENSG00000047410 TPR HNSC 0.00043 low
ENSG00000047410 TPR KICH 0.019 high
ENSG00000047410 TPR PCPG 0.0036 high
ENSG00000047410 TPR BRCA 0.033 high
ENSG00000047410 TPR ESCA 0.017 low
ENSG00000047410 TPR DLBC 0.0058 low
ENSG00000047410 TPR KIRC 0.00045 low
ENSG00000047410 TPR PRAD 0.015 high
ENSG00000047410 TPR TGCT 0.0027 high
ENSG00000047410 TPR BLCA 0.014 high
ENSG00000047410 TPR LAML 0.017 low
ENSG00000047410 TPR GBM 0.0053 low
ENSG00000047410 TPR SKCM 0.0021 low
ENSG00000047410 TPR CESC 0.0045 high
ENSG00000047410 TPR LIHC 0.00024 high
Ensembl ID Gene symbol Cancer CNV type -log10(q-value) G-score average amplitude frequency
ENSG00000047410 TPR READ Amp 1.100922 0.146252 0.629035 0.290909
ENSG00000047410 TPR SKCM Amp 1.194810 0.136889 0.679941 0.542234
ENSG00000047410 TPR LIHC Amp 3.507699 0.178069 0.863830 0.716216
ENSG00000047410 TPR DLBC Amp 2.314444 0.342879 0.614908 0.333333
ENSG00000047410 TPR BLCA Amp 1.786699 0.202862 0.511762 0.387255
ENSG00000047410 TPR BRCA Amp 4.342084 0.203391 0.769136 0.736111
ENSG00000047410 TPR OV Amp 1.559280 0.359968 0.682001 0.530225