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Translation Factor: CIRBP (NCBI Gene ID:1153) |
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Gene Summary |
Gene Information | Gene Name: CIRBP | Gene ID: 1153 | Gene Symbol | CIRBP | Gene ID | 1153 |
Gene Name | cold inducible RNA binding protein | |
Synonyms | CIRP | |
Cytomap | 19p13.3 | |
Type of Gene | protein-coding | |
Description | cold-inducible RNA-binding proteinA18 hnRNPglycine-rich RNA binding proteintesticular tissue protein Li 39 | |
Modification date | 20200327 | |
UniProtAcc | Q14011 |
Child GO biological process term(s) under GO:0006412 |
GO ID | GO term |
GO:0017148 | Negative regulation of translation |
GO:0006417 | Regulation of translation |
GO:0045727 | Positive regulation of translation |
GO:0006412 | Translation |
Gene ontology of translaction factor with evidence of Inferred from Direct Assay (IDA) from Entrez |
Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | CIRBP | GO:0009411 | response to UV | 11574538 |
Hgene | CIRBP | GO:0045727 | positive regulation of translation | 11574538 |
Hgene | CIRBP | GO:0048255 | mRNA stabilization | 11574538 |
Inferred gene age of translation factor. |
Gene | Inferred gene age group among (0 - 67.6], (67.6 - 355.7], (355.7 - 733], (733 - 1119.25], >1119.25 |
CIRBP | (0 - 67.6] |
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We searched PubMed using 'CIRBP[title] AND translation [title] AND human.' |
Gene | Title | PMID |
CIRBP | . | . |
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Skipped exons in TCGA and GTEx based on Ensembl gene isoform structure. * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. For more annotations, please visit our ExonSkipDB. |
Open reading frame (ORF) analsis of exon skipping events based on Ensembl gene isoform structure. * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
ENST | Exon skip start (DNA) | Exon Skip end (DNA) | ORF |
ENST00000586472 | 1270878 | 1270881 | 5UTR-5UTR |
ENST00000320936 | 1270926 | 1271035 | 5CDS-5UTR |
ENST00000320936 | 1271138 | 1271245 | Frame-shift |
ENST00000585630 | 1271138 | 1271245 | Frame-shift |
ENST00000586472 | 1271138 | 1271245 | Frame-shift |
ENST00000588030 | 1271138 | 1271245 | Frame-shift |
ENST00000588090 | 1271138 | 1271245 | Frame-shift |
ENST00000320936 | 1271327 | 1271466 | Frame-shift |
ENST00000585630 | 1271327 | 1271466 | Frame-shift |
ENST00000586472 | 1271327 | 1271466 | Frame-shift |
ENST00000588030 | 1271327 | 1271466 | Frame-shift |
ENST00000588090 | 1271327 | 1271466 | Frame-shift |
ENST00000320936 | 1271549 | 1271631 | Frame-shift |
ENST00000585630 | 1271549 | 1271631 | Frame-shift |
ENST00000586472 | 1271549 | 1271631 | Frame-shift |
ENST00000588030 | 1271549 | 1271631 | Frame-shift |
ENST00000588090 | 1271549 | 1271631 | Frame-shift |
Exon skipping position in the amino acid sequence. |
ENST | Exon skip start (DNA) | Exon Skip end (DNA) | Len(transcript seq) | Exon skip start (mRNA) | Exon Skip end (mRNA) | Len(amino acid seq) | Exon skip start (AA) | Exon Skip end (AA) |
Potentially (partially) lost protein functional features of UniProt. |
UniProtAcc | Exon skip start (AA) | Exon Skip end (AA) | Function feature start (AA) | Function feature end (AA) | Functional feature type | Functional feature desc. |
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Gene expression level across TCGA pancancer |
Gene expression level across GTEx pantissue |
Expression level of gene isoforms across TCGA pancancer |
Expression level of gene isoforms across GTEx pantissue |
Cancer(tissue) type-specific expression level of Translation factor using z-score distriution |
Differential expression between tumor and matched normal (in the cancer types with more than 10 matched samples) |
Cancer type | Translation factor | FC | adj.pval |
ESCA | CIRBP | 1.73045008166292 | 0.001953125 |
UCEC | CIRBP | -3.75329590281869 | 0.015625 |
HNSC | CIRBP | 2.17717956644096 | 1.15819602797274e-08 |
STAD | CIRBP | 1.13528511805511 | 4.5965425670147e-06 |
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Translation factor expression regulation through miRNA binding |
Cancer type | Gene | miRNA | TargetScan binding score (Context++ score percentile) | Coefficient | Pvalue |
Translation factor expression regulation through methylation in the promoter of Translation factor |
Cancer type | Gene | methyl group b | methyl group a | DEG pval | avg methyl in b | avg methyl in a | avg exp in b | avg exp in a |
PRAD | CIRBP | 2 | 1 | 0.0241696794267355 | 0.254677823829477 | 0.185391800356506 | -0.206959760660595 | -0.109029075761373 |
Translation factor expression regulation through methylation in the gene body of Translation factor (positive regulation) |
Cancer type | Gene | methyl group b | methyl group a | DEG pval | avg methyl in b | avg methyl in a | avg exp in b | avg exp in a |
Translation factor expression regulation through copy number variation of Translation factor |
Cancer type | Gene | Coefficient | Pvalue |
BRCA | CIRBP | -0.092325091 | 0.000573614 |
ESCA | CIRBP | 0.022738975 | 0.046083447 |
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Strongly correlated genes belong to cellular important gene groups with CIRBP (coefficient>0.8, pval<0.05, node color based on FC between tumor and matched normal). Significantly associated important genes in the individual cancer types. * Cell metabolism gene: cell metabolism genes from REACTOME (black edge), IUPHAR: drug target genes from IUPHAR (blue edge), Kinase: human kinase genes (brown edge), CGC: cancer gene census genes (orange edge), TSG: tumor suppresor genes (purple edge), Epifactor: epigenetic factors (light blue edge), TF: transcription factors (green) |
Cancer type | Gene group | Translation factor | Correlated gene | Coefficient | Pvalue |
CHOL | TF | CIRBP | AKAP8L | 0.819088849 | 6.12E-12 |
PAAD | CGC | CIRBP | CRTC1 | 0.816672831 | 4.42E-45 |
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Protein 3D structure Visit iCn3D. |
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Protein-protein interaction networks * Overlap between up-regulated DEGs (log2FC<-1 and adj.P<0.05) and STRING PPI network (center: Translation factor, node: DEGs, edges: weighted by -log2(adj.P)) |
Overlap between down-regulated DEGs (log2FC>1 and adj.P<0.05) and STRING PPI network (center: Translation factor, node: DEGs, edges: weighted by -log2(adj.P)) |
* Edge colors based on TCGA cancer types. |
* Overlap between DEGs (log2FC>1 and adj.P<0.05) and STRING PPI network per cancer (center: Translation factor, node: DEGs, node color: log2FC, edges: weighted by -log2(adj.P)) |
Cancer type | Translation factor | Interacting protein coding gene | FC | adj.pval |
KICH | CIRBP | KHDRBS1 | 1.17772583331594 | 0.000329077243804932 |
THCA | CIRBP | SF3A2 | -1.93870887642027 | 0.000619324585728192 |
ESCA | CIRBP | TREM1 | -4.33904642768857 | 0.0009765625 |
BLCA | CIRBP | KHDRBS2 | 3.42430670691912 | 0.00123013955537317 |
ESCA | CIRBP | KHDRBS1 | -2.75522662903328 | 0.001953125 |
ESCA | CIRBP | SNRPA | -3.71939307836743 | 0.001953125 |
STAD | CIRBP | TREM1 | -4.53649697763694 | 0.00361521635204554 |
CHOL | CIRBP | KHDRBS1 | -7.55107648665827 | 0.00390625 |
KICH | CIRBP | EIF4G1 | -1.46656081150743 | 0.00612920522689819 |
HNSC | CIRBP | TLR4 | 1.08212729615449 | 0.00633394569399571 |
THCA | CIRBP | HNRNPK | -8.73422542563389 | 0.00797530353045887 |
BLCA | CIRBP | KHDRBS1 | 1.32581860517507 | 0.0159721374511719 |
PRAD | CIRBP | SNRPA | -2.99222999291193 | 0.0219987445973693 |
UCEC | CIRBP | HNRNPK | 1.64532744504864 | 0.03125 |
UCEC | CIRBP | SNRPA | 1.4162366960911 | 0.046875 |
STAD | CIRBP | KHDRBS1 | -1.78849439102141 | 1.10594555735588e-06 |
KICH | CIRBP | SF3A2 | -1.42006978796939 | 1.23381614685059e-05 |
LIHC | CIRBP | SF3A2 | -1.60389783851862 | 1.52957264107439e-06 |
KIRC | CIRBP | TREM1 | -2.98926135232614 | 1.67069036077484e-10 |
BRCA | CIRBP | TLR4 | -2.36756332054809 | 1.98933887545542e-21 |
BRCA | CIRBP | TREM1 | -2.57843077227413 | 2.72905504735239e-10 |
KIRP | CIRBP | SF3A2 | -1.22971580768579 | 3.17529775202275e-05 |
LUAD | CIRBP | TLR4 | -1.79787693841954 | 3.64231156321954e-09 |
LUAD | CIRBP | KHDRBS2 | -1.77012295492985 | 3.79251210274868e-11 |
LIHC | CIRBP | SNRPA | -1.48880962162522 | 4.13231748257069e-06 |
LUAD | CIRBP | SNRPA | -1.36395233835103 | 4.39225939988757e-09 |
KIRP | CIRBP | SNRPA | -1.04126636141457 | 6.79492950439454e-06 |
LUSC | CIRBP | TREM1 | -1.38766938769506 | 7.13549502039471e-10 |
THCA | CIRBP | KHDRBS2 | -1.21153859817019 | 7.50861561019654e-11 |
Protein-protein interactors with this translation factor (BIOGRID-3.4.160) |
PPI interactors with CIRBP |
RBMX, LXN, PRMT1, ELAVL1, SF3A2, CUL3, CUL5, CUL2, CUL1, COPS5, CAND1, NEDD8, PRNP, ATXN1, APP, SF1, RTN4, CNOT3, PRKAR2A, LSM14A, TPR, KHSRP, GTF2F1, NUP88, CAPRIN1, TMPO, HNRNPH2, POLR1C, LOC100132057, BARD1, PAXIP1, SMURF1, FN1, HNRNPA0, HNRNPK, KHDRBS1, CSNK2A1, IL7R, SRF, BAG5, PARK2, RBMY1A1, SNRPA, LNX1, RBMY1F, KHDRBS2, MOV10, NXF1, RNF2, BMI1, ESR1, CCNB2, ZFAND6, NAA20, NARS, AHSA1, HNRNPA1, ORC1, PLK1, NOP56, PAPOLA, Cbx4, Junb, Rad54l, Rpl35, Trappc8, Nrip3, Bag2, NANOG, RC3H1, EGFR, CDC14B, DUSP23, PRMT5, COPRS, RIOK1, YARS2, NGRN, PAIP2B, PRMT6, MRPL1, WDR77, MALSU1, FOXA1, FBXO7, PTCH1, CUL4B, EFTUD2, ESR2, HEXIM1, MEPCE, LARP7, DPF2, RECQL4, TP53BP1, KIAA1429, PHB, APEX1, SNRNP70, NFX1, CMTR1, SRSF3, ARIH2, OBSL1, ZC3H18, BRIX1, CHMP4C, ARHGAP22, ARHGAP19, ARHGAP35, DOCK3, DOCK9, MCF2L2, NGEF, PLEKHG3, PLEKHG7, INS, MAFB, PTEN, Apc2, FBP1, KDM4D, WDR48, BRD1, TDRD7, WDR20, USP1, USP46, DDX58, UFL1, DDRGK1, FZR1, WDR5, MAP4K2, TNPO3, MCAT, ANGEL2, FASTKD2, MTERF3, PRMT8, CLNS1A, BCL2L12, SOX6, |
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Clinically associated variants from ClinVar. |
Gene | Chr | Position | RefSeq | VarSeq | RefSeeq | VarType | Pathogenic | Disease | VarInfo |
CIRBP | chr19 | 1271129 | C | T | single_nucleotide_variant | Benign | not_provided | SO:0001627|intron_variant | SO:0001627|intron_variant |
CIRBP | chr19 | 1272187 | C | G | single_nucleotide_variant | Benign | not_provided | SO:0001619|non-coding_transcript_variant,SO:0001819|synonymous_variant,SO:0001627|intron_variant | SO:0001619|non-coding_transcript_variant,SO:0001819|synonymous_variant,SO:0001627|intron_variant |
nsSNVs with sample frequency (size of circle) from TCGA 33 cancers. |
SNVs and Indels |
Gene | Cancer type | Chromosome | Start | End | RefSeeq | MutSeq | Mutation type | AAchange | # samples |
CIRBP | BRCA | chr19 | 1272368 | 1272368 | G | A | Missense_Mutation | p.V240M | 4 |
CIRBP | BRCA | chr19 | 1272041 | 1272041 | G | A | Missense_Mutation | p.D165N | 3 |
CIRBP | BRCA | chr19 | 1272339 | 1272339 | G | A | Missense_Mutation | p.R230H | 3 |
CIRBP | BRCA | chr19 | 1272581 | 1272581 | A | C | RNA | NULL | 3 |
CIRBP | UCEC | chr19 | 1271416 | 1271416 | G | A | Missense_Mutation | p.G100D | 3 |
CIRBP | CESC | chr19 | 1272191 | 1272191 | C | G | Missense_Mutation | p.Q162E | 2 |
CIRBP | UCEC | chr19 | 1270880 | 1270880 | T | C | RNA | NULL | 2 |
CIRBP | UCEC | chr19 | 1271392 | 1271392 | G | A | Missense_Mutation | p.G92E | 2 |
CIRBP | BRCA | chr19 | 1271007 | 1271007 | C | G | Missense_Mutation | p.S8C | 2 |
CIRBP | PRAD | chr19 | 1271165 | 1271165 | C | T | Nonsense_Mutation | p.Q44* | 2 |
CIRBP | UCEC | chr19 | 1272297 | 1272297 | G | A | Missense_Mutation | p.R216K | 2 |
CIRBP | LIHC | chr19 | 1271158 | 1271158 | G | C | Missense_Mutation | 2 | |
CIRBP | BRCA | chr19 | 1272306 | 1272306 | C | G | Missense_Mutation | p.S219C | 2 |
CIRBP | LUAD | chr19 | 1270962 | 1270962 | T | G | Silent | p.V10V | 2 |
CIRBP | UCEC | chr19 | 1272432 | 1272434 | ACA | - | In_Frame_Del | p.N171in_frame_del | 2 |
CIRBP | BRCA | chr19 | 1272448 | 1272448 | C | G | RNA | NULL | 2 |
CIRBP | SKCM | chr19 | 1270987 | 1270987 | G | A | Missense_Mutation | p.E19K | 2 |
CIRBP | UCEC | chr19 | 1272472 | 1272472 | A | G | RNA | NULL | 2 |
CIRBP | LIHC | chr19 | 1271158 | 1271158 | G | C | Missense_Mutation | p.R41S | 2 |
CIRBP | CESC | chr19 | 1271030 | 1271030 | C | T | Missense_Mutation | 2 | |
CIRBP | BLCA | chr19 | 1272166 | 1272166 | C | T | Silent | 1 | |
CIRBP | KIRP | chr19 | 1272031 | 1272031 | A | C | Missense_Mutation | p.R161S | 1 |
CIRBP | UCEC | chr19 | 1272432 | 1272434 | ACA | - | In_Frame_Del | p.N171del | 1 |
CIRBP | BLCA | chr19 | 1271439 | 1271439 | C | T | Nonsense_Mutation | p.R55* | 1 |
CIRBP | LIHC | chr19 | 1272316 | 1272317 | - | G | Frame_Shift_Ins | p.WG203fs | 1 |
CIRBP | MESO | chr19 | 1271574 | 1271574 | G | A | Missense_Mutation | p.G72E | 1 |
CIRBP | UCEC | chr19 | 1271570 | 1271570 | G | - | Frame_Shift_Del | p.G124fs | 1 |
CIRBP | BLCA | chr19 | 1271019 | 1271019 | C | T | Missense_Mutation | 1 | |
CIRBP | KIRP | chr19 | 1272265 | 1272266 | - | G | Frame_Shift_Ins | p.A187fs | 1 |
CIRBP | BLCA | chr19 | 1270999 | 1270999 | G | A | Missense_Mutation | p.E23K | 1 |
CIRBP | LIHC | chr19 | 1270955 | 1270955 | T | - | Frame_Shift_Del | p.L8fs | 1 |
CIRBP | CESC | chr19 | 1271012 | 1271012 | C | T | Missense_Mutation | 1 | |
CIRBP | PAAD | chr19 | 1271535 | 1271535 | T | G | Missense_Mutation | 1 | |
CIRBP | BLCA | chr19 | 1272363 | 1272363 | C | A | Missense_Mutation | 1 | |
CIRBP | LIHC | chr19 | 1272372 | 1272372 | A | G | Missense_Mutation | 1 | |
CIRBP | BLCA | chr19 | 1271019 | 1271019 | C | T | Silent | p.Y29Y | 1 |
CIRBP | LIHC | chr19 | 1272397 | 1272397 | T | - | Frame_Shift_Del | p.P230fs | 1 |
CIRBP | CESC | chr19 | 1271012 | 1271012 | C | T | Nonsense_Mutation | p.Q10* | 1 |
CIRBP | PRAD | chr19 | 1271165 | 1271165 | C | T | Nonsense_Mutation | p.Q44X | 1 |
CIRBP | BLCA | chr19 | 1272370 | 1272370 | G | T | Silent | 1 | |
CIRBP | LIHC | chr19 | 1272316 | 1272317 | - | - | Frame_Shift_Ins | 1 | |
CIRBP | LIHC | chr19 | 1271998 | 1271998 | C | - | Frame_Shift_Del | p.G97fs | 1 |
CIRBP | CESC | chr19 | 1271030 | 1271030 | C | T | Missense_Mutation | p.S33F | 1 |
CIRBP | BLCA | chr19 | 1272373 | 1272373 | G | T | Missense_Mutation | 1 | |
CIRBP | ESCA | chr19 | 1270889 | 1270889 | A | T | Missense_Mutation | 1 | |
CIRBP | SARC | chr19 | 1271446 | 1271446 | G | T | Missense_Mutation | 1 | |
CIRBP | STAD | chr19 | 1272159 | 1272159 | G | A | Missense_Mutation | p.C151Y | 1 |
CIRBP | BLCA | chr19 | 1272166 | 1272166 | C | T | Silent | p.C153C | 1 |
CIRBP | LIHC | chr19 | 1271184 | 1271184 | G | T | Missense_Mutation | 1 | |
CIRBP | LUAD | chr19 | 1272346 | 1272346 | G | A | Silent | p.P213P | 1 |
CIRBP | HNSC | chr19 | 1271983 | 1271983 | G | A | Silent | 1 | |
CIRBP | STAD | chr19 | 1271433 | 1271433 | G | - | Frame_Shift_Del | p.G106fs | 1 |
CIRBP | BLCA | chr19 | 1270999 | 1270999 | G | A | Nonsense_Mutation | p.W5* | 1 |
CIRBP | LIHC | chr19 | 1270937 | 1270937 | C | T | Missense_Mutation | 1 | |
CIRBP | LUAD | chr19 | 1272009 | 1272009 | G | A | Missense_Mutation | p.R101Q | 1 |
CIRBP | HNSC | chr19 | 1271529 | 1271529 | C | T | Missense_Mutation | 1 | |
CIRBP | SKCM | chr19 | 1272063 | 1272063 | C | T | Missense_Mutation | p.S119F | 1 |
CIRBP | THYM | chr19 | 1271392 | 1271392 | G | T | Missense_Mutation | p.G92V | 1 |
CIRBP | BLCA | chr19 | 1271019 | 1271019 | C | T | Missense_Mutation | p.T12M | 1 |
CIRBP | LIHC | chr19 | 1271998 | 1271998 | C | - | Frame_Shift_Del | 1 | |
CIRBP | LUAD | chr19 | 1272339 | 1272339 | G | T | Missense_Mutation | p.R211L | 1 |
CIRBP | HNSC | chr19 | 1271989 | 1271989 | G | C | Missense_Mutation | 1 | |
CIRBP | STAD | chr19 | 1271433 | 1271433 | G | - | Frame_Shift_Del | p.R105fs | 1 |
CIRBP | THYM | chr19 | 1270978 | 1270978 | G | A | Missense_Mutation | 1 | |
CIRBP | BLCA | chr19 | 1272363 | 1272363 | C | A | Missense_Mutation | p.S219Y | 1 |
CIRBP | LIHC | chr19 | 1271998 | 1271998 | C | - | Frame_Shift_Del | p.G150fs | 1 |
CIRBP | LUSC | chr19 | 1271175 | 1271175 | G | T | Missense_Mutation | p.R47L | 1 |
CIRBP | HNSC | chr19 | 1271983 | 1271983 | G | A | Silent | p.R92R | 1 |
CIRBP | THYM | chr19 | 1270978 | 1270978 | G | A | Missense_Mutation | p.D16N | 1 |
CIRBP | LIHC | chr19 | 1271585 | 1271585 | G | A | Missense_Mutation | p.E129K | 1 |
CIRBP | BLCA | chr19 | 1272370 | 1272370 | G | T | Silent | p.V221V | 1 |
CIRBP | LUSC | chr19 | 1271623 | 1271623 | C | A | Nonsense_Mutation | p.Y141* | 1 |
CIRBP | HNSC | chr19 | 1271989 | 1271989 | G | C | Missense_Mutation | p.Q94H | 1 |
CIRBP | BLCA | chr19 | 1272373 | 1272373 | G | T | Missense_Mutation | p.K222N | 1 |
CIRBP | MESO | chr19 | 1271574 | 1271574 | G | A | Missense_Mutation | 1 |
Copy number variation (CNV) of CIRBP * Click on the image to open the original image in a new window. |
Fusion gene breakpoints (product of the structural variants (SVs)) across CIRBP * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
Fusion genes with this translation factor from FusionGDB2.0. |
FusionGDB2 ID | Disease | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
90505 | BLCA | TCGA-FD-A3B6-01A | ABCA7 | chr19 | 1049436 | + | CIRBP | chr19 | 1264252 | + |
89761 | PAAD | TCGA-FB-AAQ2-01A | CIRBP | chr19 | 1272050 | + | APC2 | chr19 | 1465154 | + |
90505 | N/A | AW592560 | CIRBP | chr19 | 1271377 | + | CIRBP | chr19 | 1270937 | + |
90505 | N/A | CN478954 | CIRBP | chr19 | 1273098 | - | CIRBP | chr19 | 1272962 | + |
92023 | BLCA | TCGA-4Z-AA87-01A | CIRBP | chr19 | 1269409 | - | CNN2 | chr19 | 1031070 | + |
72743 | STAD | TCGA-D7-A6EZ-01A | CIRBP | chr19 | 1269409 | + | ERAS | chrX | 48687491 | + |
68205 | N/A | BI493512 | CIRBP | chr19 | 1273171 | + | KIDINS220 | chr2 | 8927881 | - |
102996 | STAD | TCGA-D7-8574-01A | CIRBP | chr19 | 1269409 | + | MISP | chr19 | 756890 | + |
102709 | N/A | BP228603 | CIRBP | chr19 | 1271418 | + | OBSCN | chr1 | 228493832 | + |
85745 | N/A | DA500684 | CIRBP | chr19 | 1271411 | + | PKNOX1 | chr21 | 44450156 | + |
75728 | Non-Cancer | ERR315406 | CIRBP | chr19 | 1269409 | + | RNF166 | chr16 | 88767826 | - |
79376 | LUAD | TCGA-91-6831-01A | CIRBP | chr19 | 1269409 | + | WDR18 | chr19 | 994019 | + |
78099 | STAD | TCGA-BR-A4QL | CIRBP | chr19 | 1272050 | + | WNK2 | chr9 | 96079801 | + |
92845 | STAD | TCGA-D7-A4Z0-01A | CIRBP | chr19 | 1272050 | + | ZC3HAV1 | chr7 | 138774505 | - |
90505 | GBM | TCGA-19-A6J5-01A | COL6A1 | chr21 | 47401861 | + | CIRBP | chr19 | 1270927 | + |
90505 | N/A | AA570603 | ESRRB | chr14 | 76778316 | - | CIRBP | chr19 | 1273171 | - |
90505 | STAD | TCGA-BR-8364-01A | KLHL24 | chr3 | 183353581 | + | CIRBP | chr19 | 1270927 | + |
90505 | N/A | BG698664 | PNLIPRP3 | chr10 | 118202646 | + | CIRBP | chr19 | 1271412 | + |
90510 | THCA | TCGA-EM-A22K | TGIF2 | chr20 | 35201927 | + | CIRBP | chr19 | 1270926 | + |
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Kaplan-Meier plots with logrank tests of overall survival (OS) |
Cancer type | Translation factor | Coefficent | Hazard ratio | Wald test pval | Likelihool ratio pval | Logrank test pval | # samples |
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Differential gene expression between female and male. (Wilcoxon test, pval<0.05) |
Cancer type | Translation factor | pval | adj.p |
KIRP | CIRBP | 0.000348950152397787 | 0.0098 |
LUAD | CIRBP | 0.0167842595627881 | 0.45 |
LIHC | CIRBP | 0.0182566113569019 | 0.47 |
TGCT | CIRBP | 0.0343711046163315 | 0.86 |
LAML | CIRBP | 0.045303963041518 | 1 |
THCA | CIRBP | 0.0492148314085869 | 1 |
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Differential gene expression between young and old age groups (Wilcoxon test, pval<0.05) |
Cancer type | Translation factor | pval | adj.p |
LGG | CIRBP | 0.0313117410264964 | 0.94 |
BRCA | CIRBP | 0.00279436673842149 | 0.092 |
ESCA | CIRBP | 0.00947190834668049 | 0.29 |
SARC | CIRBP | 0.00858797139069876 | 0.27 |
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Drugs targeting genes involved in this translation factor. (DrugBank Version 5.1.8 2021-05-08) |
UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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Diseases associated with this translation factor. (DisGeNet 4.0) |
Disease ID | Disease Name | # PubMeds | Disease source |
C0151744 | Myocardial Ischemia | 1 | CTD_human |
C0600467 | Neurogenic Inflammation | 1 | CTD_human |
C0751865 | Alcohol-Induced Disorders, Nervous System | 1 | CTD_human |
C1510586 | Autism Spectrum Disorders | 1 | CTD_human |