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Gene: C11orf54 |
Gene summary for C11ORF54 |
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Gene information | Species | Human | Gene symbol | C11orf54 | Gene ID | 28970 |
Gene name | chromosome 11 open reading frame 54 | |
Gene Alias | PTD012 | |
Cytomap | 11q21 | |
Gene Type | protein-coding | GO ID | GO:0005575 | UniProtAcc | A0A024R396 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
28970 | C11orf54 | P15T-E | Human | Esophagus | ESCC | 1.73e-08 | 9.18e-02 | 0.1149 |
28970 | C11orf54 | P16T-E | Human | Esophagus | ESCC | 3.52e-17 | 2.93e-01 | 0.1153 |
28970 | C11orf54 | P17T-E | Human | Esophagus | ESCC | 2.99e-07 | 2.26e-01 | 0.1278 |
28970 | C11orf54 | P20T-E | Human | Esophagus | ESCC | 1.37e-09 | 1.13e-01 | 0.1124 |
28970 | C11orf54 | P21T-E | Human | Esophagus | ESCC | 2.19e-22 | 2.41e-01 | 0.1617 |
28970 | C11orf54 | P22T-E | Human | Esophagus | ESCC | 1.30e-04 | 2.21e-02 | 0.1236 |
28970 | C11orf54 | P23T-E | Human | Esophagus | ESCC | 8.00e-11 | 2.08e-01 | 0.108 |
28970 | C11orf54 | P24T-E | Human | Esophagus | ESCC | 1.19e-04 | 3.40e-02 | 0.1287 |
28970 | C11orf54 | P26T-E | Human | Esophagus | ESCC | 3.64e-20 | 2.89e-01 | 0.1276 |
28970 | C11orf54 | P27T-E | Human | Esophagus | ESCC | 1.01e-17 | 1.43e-01 | 0.1055 |
28970 | C11orf54 | P28T-E | Human | Esophagus | ESCC | 6.63e-09 | 1.93e-01 | 0.1149 |
28970 | C11orf54 | P30T-E | Human | Esophagus | ESCC | 1.61e-09 | 4.38e-01 | 0.137 |
28970 | C11orf54 | P31T-E | Human | Esophagus | ESCC | 3.27e-13 | 2.13e-01 | 0.1251 |
28970 | C11orf54 | P32T-E | Human | Esophagus | ESCC | 7.24e-10 | 1.40e-01 | 0.1666 |
28970 | C11orf54 | P37T-E | Human | Esophagus | ESCC | 1.42e-04 | 9.54e-02 | 0.1371 |
28970 | C11orf54 | P39T-E | Human | Esophagus | ESCC | 2.28e-11 | 8.18e-02 | 0.0894 |
28970 | C11orf54 | P40T-E | Human | Esophagus | ESCC | 1.02e-02 | 6.32e-02 | 0.109 |
28970 | C11orf54 | P42T-E | Human | Esophagus | ESCC | 8.17e-09 | 1.77e-01 | 0.1175 |
28970 | C11orf54 | P44T-E | Human | Esophagus | ESCC | 5.92e-04 | 8.44e-02 | 0.1096 |
28970 | C11orf54 | P48T-E | Human | Esophagus | ESCC | 1.77e-03 | 1.86e-02 | 0.0959 |
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∗log2FC in expression of this searched gene in stem-like cells from each diseased tissue sample relative to stem-like cells in normal samples in each tissue plotted against the malignancy continuum. Samples are colored based on if they are from different disease stage. |
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Malignant transformation related pathway analysis |
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Tissue | Disease Stage | Enriched GO biological Processes |
Colorectum | AD | ![]() |
Colorectum | SER | ![]() |
Colorectum | MSS | ![]() |
Colorectum | MSI-H | ![]() |
Colorectum | FAP | ![]() |
∗Top 15 enriched GO BP terms are showed in the bar plot of each disease state in each tissue. Each row represents a significant GO biological process which is colored according to the -log10(p.adjust). |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
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Cell-cell communication analysis |
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Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
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Single-cell gene regulatory network inference analysis |
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TF | Cell Type | Tissue | Disease Stage | Target Gene | RSS | Regulon Activity |
∗The dot plots of a searched regulon are shown for all cell subpopulations in each disease state of each tissue based on the regulon specific score inferred using pySCENIC and by calculating the average expression. |
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Somatic mutation of malignant transformation related genes |
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Hugo Symbol | Variant Class | Variant Classification | dbSNP RS | HGVSc | HGVSp | HGVSp Short | SWISSPROT | BIOTYPE | SIFT | PolyPhen | Tumor Sample Barcode | Tissue | Histology | Sex | Age | Stage | Therapy Types | Drugs | Outcome |
C11orf54 | SNV | Missense_Mutation | novel | c.773N>G | p.Pro258Arg | p.P258R | Q9H0W9 | protein_coding | deleterious(0.02) | probably_damaging(0.988) | TCGA-A2-A0CR-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | adriamycin | CR |
C11orf54 | SNV | Missense_Mutation | c.328G>C | p.Glu110Gln | p.E110Q | Q9H0W9 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-C5-A3HE-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | PD | |
C11orf54 | SNV | Missense_Mutation | rs780612413 | c.101N>T | p.Ser34Phe | p.S34F | Q9H0W9 | protein_coding | deleterious(0.01) | possibly_damaging(0.782) | TCGA-VS-A959-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Unknown | Unknown | SD |
C11orf54 | SNV | Missense_Mutation | c.445N>G | p.Cys149Gly | p.C149G | Q9H0W9 | protein_coding | tolerated(0.33) | benign(0.059) | TCGA-AG-3892-01 | Colorectum | rectum adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
C11orf54 | deletion | Frame_Shift_Del | c.810delT | p.Phe270LeufsTer18 | p.F270Lfs*18 | Q9H0W9 | protein_coding | TCGA-AA-3864-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |||
C11orf54 | deletion | Frame_Shift_Del | c.810delT | p.Phe270LeufsTer18 | p.F270Lfs*18 | Q9H0W9 | protein_coding | TCGA-AZ-4615-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | xeloda | PD | |||
C11orf54 | SNV | Missense_Mutation | novel | c.856N>T | p.Asp286Tyr | p.D286Y | Q9H0W9 | protein_coding | deleterious(0) | probably_damaging(0.957) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
C11orf54 | SNV | Missense_Mutation | novel | c.145N>T | p.Pro49Ser | p.P49S | Q9H0W9 | protein_coding | tolerated(0.26) | benign(0.245) | TCGA-A5-A1OF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
C11orf54 | SNV | Missense_Mutation | novel | c.590N>A | p.Gly197Glu | p.G197E | Q9H0W9 | protein_coding | tolerated(0.12) | probably_damaging(0.983) | TCGA-A5-A1OF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
C11orf54 | SNV | Missense_Mutation | rs371075089 | c.904N>T | p.Arg302Cys | p.R302C | Q9H0W9 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-AP-A056-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
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Related drugs of malignant transformation related genes |
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(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
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