Ensembl ID ENSG00000163902 Gene ID 6184 Accession 10381
Gene Symbol RPN1 Alias OST1;RBPH1 Full Name ribophorin I
Position 3 : 128619969 - 128681075 Length 61107 bases Strand Minus strand
Status Confidence Main interacting RNAsN.A.RBP type Non-canonical_RBPs
Summary This gene encodes a type I integral membrane protein found only in the rough endoplasmic reticulum. The encoded protein is part of an N-oligosaccharyl transferase complex that links high mannose oligosaccharides to asparagine residues found in the Asn-X-Ser/Thr consensus motif of nascent polypeptide chains. This protein forms part of the regulatory subunit of the 26S proteasome and may mediate binding of ubiquitin-like domains to this proteasome. [provided by RefSeq, Jul 2008]

ENSG00000163902 Expression In 33 Tumors

Ensembl ID Gene symbol Log2 Foldchange Pvaue Cancer
ENSG00000163902 RPN1 0.66 6.78e-23 HNSC
ENSG00000163902 RPN1 0.86 1.58e-14 BLCA
ENSG00000163902 RPN1 0.75 9.50e-48 BRCA
ENSG00000163902 RPN1 0.63 1.82e-16 LUSC
ENSG00000163902 RPN1 0.86 3.97e-25 UCEC
Ensembl ID Gene symbol Cancer types Pubmed ID
ENSG00000163902 RPN1 AML 14607750
ENSG00000163902 RPN1 AML with recurrent genetic abnormalities 19860179
ENSG00000163902 RPN1 non-small cell lung cancers 20193080
ENSG00000163902 RPN1 tumor 21408220
ENSG00000163902 RPN1 tumor 21602888
ENSG00000163902 RPN1 kidney cancer 21634111
ENSG00000163902 RPN1 pancreatic tumor 24471499
ENSG00000163902 RPN1 AML 25794001
ENSG00000163902 RPN1 AML 26237023
ENSG00000163902 RPN1 bladder cancer 27034531
ENSG00000163902 RPN1 cancer 27171286
ENSG00000163902 RPN1 AML 27542247
ENSG00000163902 RPN1 AML without maturation 28977979
ENSG00000163902 RPN1 cancer 30881377
ENSG00000163902 RPN1 esophageal cancer 30940778
ENSG00000163902 RPN1 AMLs 9192861
Ensembl ID Gene symbol Disease/phenotype Mutation type Mutated / Total samples Literature
ENSG00000163902 RPN1 colon adenocarcinoma sequence_alteration 0.9695% (7/722) 1 entry
ENSG00000163902 RPN1 chronic lymphocytic leukemia sequence_alteration 0.3378% (3/888) 1 entry
ENSG00000163902 RPN1 brain glioblastoma sequence_alteration 0.216% (2/926) 1 entry
ENSG00000163902 RPN1 skin melanoma missense_variant 0.9307% (9/967) 2 entries
ENSG00000163902 RPN1 embryonal rhabdomyosarcoma missense_variant 2.632% (2/76) 1 entry
ENSG00000163902 RPN1 prostate carcinoma sequence_alteration 1.405% (6/427) 1 entry
ENSG00000163902 RPN1 esophageal squamous cell carcinoma sequence_alteration 0.5926% (4/675) 2 entries
ENSG00000163902 RPN1 skin melanoma sequence_alteration 0.9307% (9/967) 1 entry
ENSG00000163902 RPN1 colon adenocarcinoma missense_variant 0.9695% (7/722) 3 entries
ENSG00000163902 RPN1 clear cell renal carcinoma sequence_alteration 0.4354% (6/1378) 2 entries
ENSG00000163902 RPN1 embryonal rhabdomyosarcoma sequence_alteration 2.632% (2/76) 1 entry
ENSG00000163902 RPN1 clear cell renal carcinoma missense_variant 0.4354% (6/1378) 2 entries
ENSG00000163902 RPN1 female breast carcinoma sequence_alteration 0.7491% (2/267) 1 entry
ENSG00000163902 RPN1 esophageal squamous cell carcinoma missense_variant 0.5926% (4/675) 3 entries
ENSG00000163902 RPN1 colorectal adenocarcinoma sequence_alteration 2.197% (25/1138) 2 entries
ENSG00000163902 RPN1 colorectal adenocarcinoma missense_variant 2.197% (25/1138) 3 entries
ENSG00000163902 RPN1 lung adenocarcinoma missense_variant 0.5159% (6/1163) 3 entries
ENSG00000163902 RPN1 colorectal adenocarcinoma frameshift_variant 2.197% (25/1138) 1 entry
ENSG00000163902 RPN1 gastric adenocarcinoma missense_variant 0.8961% (5/558) 1 entry
ENSG00000163902 RPN1 colon carcinoma missense_variant 12.5% (1/8) 1 entry
ENSG00000163902 RPN1 Breast Carcinoma by Gene Expression Profile missense_variant 5.263% (1/19) 1 entry
ENSG00000163902 RPN1 Brain Stem Glioblastoma sequence_alteration 1.786% (1/56) 1 entry
ENSG00000163902 RPN1 ovarian serous adenocarcinoma frameshift_variant 0.2972% (2/673) 1 entry
ENSG00000163902 RPN1 female breast carcinoma missense_variant 0.7491% (2/267) 1 entry
ENSG00000163902 RPN1 neoplasm frameshift_variant 3.571% (1/28) 1 entry
ENSG00000163902 RPN1 Mantle cell lymphoma missense_variant 2.439% (1/41) 1 entry
ENSG00000163902 RPN1 prostate carcinoma missense_variant 1.405% (6/427) 1 entry
ENSG00000163902 RPN1 rectal adenocarcinoma sequence_alteration 0.4525% (1/221) 1 entry
ENSG00000163902 RPN1 non-small cell lung carcinoma sequence_alteration 1.887% (1/53) 1 entry
ENSG00000163902 RPN1 melanoma missense_variant 0.9901% (1/101) 1 entry
ENSG00000163902 RPN1 basal cell carcinoma missense_variant 1.724% (1/58) 1 entry
ENSG00000163902 RPN1 Gallbladder Adenocarcinoma sequence_alteration 1.149% (1/87) 1 entry
ENSG00000163902 RPN1 rectal adenocarcinoma missense_variant 0.4525% (1/221) 1 entry
ENSG00000163902 RPN1 osteosarcoma sequence_alteration 0.8621% (1/116) 1 entry
ENSG00000163902 RPN1 Merkel cell skin cancer missense_variant 3.333% (1/30) 1 entry
ENSG00000163902 RPN1 diffuse gastric adenocarcinoma missense_variant 1.266% (1/79) 1 entry
ENSG00000163902 RPN1 adenosquamous lung carcinoma missense_variant 9.091% (1/11) 1 entry
ENSG00000163902 RPN1 non-small cell lung carcinoma missense_variant 1.887% (1/53) 1 entry
ENSG00000163902 RPN1 hepatocellular carcinoma missense_variant 1.001% (9/899) 1 entry
ENSG00000163902 RPN1 ovarian serous adenocarcinoma missense_variant 0.2972% (2/673) 1 entry
ENSG00000163902 RPN1 Gallbladder Adenocarcinoma missense_variant 1.149% (1/87) 1 entry
ENSG00000163902 RPN1 metaplastic breast carcinoma missense_variant 1.961% (1/51) 1 entry
Ensembl ID Gene symbol Cancer P-value Which worse show
ENSG00000163902 RPN1 MESO 0.012 high
ENSG00000163902 RPN1 SARC 0.0083 high
ENSG00000163902 RPN1 UVM 0.047 low
ENSG00000163902 RPN1 PAAD 0.0055 high
ENSG00000163902 RPN1 ACC 0.0017 high
ENSG00000163902 RPN1 HNSC 0.017 high
ENSG00000163902 RPN1 KIRP 0.015 high
ENSG00000163902 RPN1 KICH 0.016 high
ENSG00000163902 RPN1 THYM 0.0097 low
ENSG00000163902 RPN1 BRCA 0.02 low
ENSG00000163902 RPN1 COAD 0.013 high
ENSG00000163902 RPN1 ESCA 0.0016 high
ENSG00000163902 RPN1 OV 0.022 low
ENSG00000163902 RPN1 TGCT 0.015 high
ENSG00000163902 RPN1 LAML 0.04 low
ENSG00000163902 RPN1 GBM 0.033 high
ENSG00000163902 RPN1 SKCM 0.039 low
ENSG00000163902 RPN1 CESC 0.043 low
Ensembl ID Gene symbol Cancer CNV type -log10(q-value) G-score average amplitude frequency
ENSG00000163902 RPN1 GBM Del 1.151254 0.057791 0.493485 0.093588
ENSG00000163902 RPN1 PRAD Amp 3.827518 0.088768 0.475201 0.152439