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Gene: RBM4 |
Gene summary for RBM4 |
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Gene information | Species | Human | Gene symbol | RBM4 | Gene ID | 5936 |
Gene name | RNA binding motif protein 4 | |
Gene Alias | LARK | |
Cytomap | 11q13.2 | |
Gene Type | protein-coding | GO ID | GO:0000375 | UniProtAcc | Q9BWF3 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
5936 | RBM4 | HTA11_3410_2000001011 | Human | Colorectum | AD | 1.39e-04 | 2.59e-01 | 0.0155 |
5936 | RBM4 | HTA11_2487_2000001011 | Human | Colorectum | SER | 1.64e-12 | 6.76e-01 | -0.1808 |
5936 | RBM4 | HTA11_2951_2000001011 | Human | Colorectum | AD | 9.28e-03 | 6.44e-01 | 0.0216 |
5936 | RBM4 | HTA11_1938_2000001011 | Human | Colorectum | AD | 3.51e-14 | 7.49e-01 | -0.0811 |
5936 | RBM4 | HTA11_347_2000001011 | Human | Colorectum | AD | 4.11e-12 | 5.29e-01 | -0.1954 |
5936 | RBM4 | HTA11_2112_2000001011 | Human | Colorectum | SER | 3.87e-03 | 5.78e-01 | -0.2196 |
5936 | RBM4 | HTA11_3361_2000001011 | Human | Colorectum | AD | 5.02e-04 | 6.38e-01 | -0.1207 |
5936 | RBM4 | HTA11_696_2000001011 | Human | Colorectum | AD | 2.69e-21 | 6.31e-01 | -0.1464 |
5936 | RBM4 | HTA11_866_2000001011 | Human | Colorectum | AD | 2.98e-03 | 3.49e-01 | -0.1001 |
5936 | RBM4 | HTA11_1391_2000001011 | Human | Colorectum | AD | 1.19e-14 | 8.07e-01 | -0.059 |
5936 | RBM4 | HTA11_5212_2000001011 | Human | Colorectum | AD | 1.20e-04 | 5.90e-01 | -0.2061 |
5936 | RBM4 | HTA11_546_2000001011 | Human | Colorectum | AD | 1.21e-02 | 3.68e-01 | -0.0842 |
5936 | RBM4 | HTA11_866_3004761011 | Human | Colorectum | AD | 5.83e-16 | 6.80e-01 | 0.096 |
5936 | RBM4 | HTA11_4255_2000001011 | Human | Colorectum | SER | 2.41e-02 | 6.79e-01 | 0.0446 |
5936 | RBM4 | HTA11_8622_2000001021 | Human | Colorectum | SER | 4.20e-04 | 4.29e-01 | 0.0528 |
5936 | RBM4 | HTA11_7663_2000001011 | Human | Colorectum | SER | 6.32e-05 | 7.58e-01 | 0.0131 |
5936 | RBM4 | HTA11_10623_2000001011 | Human | Colorectum | AD | 1.88e-06 | 5.81e-01 | -0.0177 |
5936 | RBM4 | HTA11_6801_2000001011 | Human | Colorectum | SER | 8.45e-03 | 6.59e-01 | 0.0171 |
5936 | RBM4 | HTA11_10711_2000001011 | Human | Colorectum | AD | 1.84e-04 | 4.36e-01 | 0.0338 |
5936 | RBM4 | HTA11_7696_3000711011 | Human | Colorectum | AD | 7.86e-08 | 4.97e-01 | 0.0674 |
Page: 1 2 3 4 5 6 7 8 9 |
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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). |
Page: 1 2 3 4 5 6 7 8 9 |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:000941621 | Skin | cSCC | response to light stimulus | 107/4864 | 320/18723 | 1.66e-03 | 1.02e-02 | 107 |
GO:00096482 | Skin | cSCC | photoperiodism | 16/4864 | 33/18723 | 4.50e-03 | 2.30e-02 | 16 |
GO:00431532 | Skin | cSCC | entrainment of circadian clock by photoperiod | 14/4864 | 29/18723 | 8.08e-03 | 3.74e-02 | 14 |
GO:0008380113 | Thyroid | PTC | RNA splicing | 273/5968 | 434/18723 | 4.44e-41 | 1.40e-37 | 273 |
GO:0002181113 | Thyroid | PTC | cytoplasmic translation | 121/5968 | 148/18723 | 4.32e-36 | 4.54e-33 | 121 |
GO:0000375113 | Thyroid | PTC | RNA splicing, via transesterification reactions | 202/5968 | 324/18723 | 6.81e-30 | 3.91e-27 | 202 |
GO:0000377113 | Thyroid | PTC | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 199/5968 | 320/18723 | 2.96e-29 | 1.44e-26 | 199 |
GO:0000398113 | Thyroid | PTC | mRNA splicing, via spliceosome | 199/5968 | 320/18723 | 2.96e-29 | 1.44e-26 | 199 |
GO:1903311112 | Thyroid | PTC | regulation of mRNA metabolic process | 181/5968 | 288/18723 | 1.60e-27 | 5.94e-25 | 181 |
GO:0032386111 | Thyroid | PTC | regulation of intracellular transport | 202/5968 | 337/18723 | 1.12e-26 | 3.93e-24 | 202 |
GO:0006913112 | Thyroid | PTC | nucleocytoplasmic transport | 181/5968 | 301/18723 | 2.93e-24 | 7.69e-22 | 181 |
GO:0051169112 | Thyroid | PTC | nuclear transport | 181/5968 | 301/18723 | 2.93e-24 | 7.69e-22 | 181 |
GO:0050684112 | Thyroid | PTC | regulation of mRNA processing | 98/5968 | 137/18723 | 1.53e-21 | 3.10e-19 | 98 |
GO:0043484113 | Thyroid | PTC | regulation of RNA splicing | 102/5968 | 148/18723 | 2.03e-20 | 3.21e-18 | 102 |
GO:0006413112 | Thyroid | PTC | translational initiation | 84/5968 | 118/18723 | 1.89e-18 | 2.09e-16 | 84 |
GO:0006417113 | Thyroid | PTC | regulation of translation | 236/5968 | 468/18723 | 2.70e-17 | 2.52e-15 | 236 |
GO:004682223 | Thyroid | PTC | regulation of nucleocytoplasmic transport | 76/5968 | 106/18723 | 4.11e-17 | 3.70e-15 | 76 |
GO:0048024113 | Thyroid | PTC | regulation of mRNA splicing, via spliceosome | 71/5968 | 101/18723 | 2.39e-15 | 1.71e-13 | 71 |
GO:0006446110 | Thyroid | PTC | regulation of translational initiation | 55/5968 | 79/18723 | 6.21e-12 | 2.63e-10 | 55 |
GO:0000380111 | Thyroid | PTC | alternative mRNA splicing, via spliceosome | 51/5968 | 77/18723 | 6.09e-10 | 1.92e-08 | 51 |
Page: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 |
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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 |
RBM4 | SNV | Missense_Mutation | c.477G>C | p.Gln159His | p.Q159H | Q9BWF3 | protein_coding | tolerated(0.33) | benign(0.007) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
RBM4 | SNV | Missense_Mutation | rs771127066 | c.1079N>A | p.Arg360Gln | p.R360Q | Q9BWF3 | protein_coding | tolerated(0.09) | probably_damaging(0.968) | TCGA-C8-A135-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | 5-fluorouracil | CR |
RBM4 | SNV | Missense_Mutation | c.286N>A | p.Ala96Thr | p.A96T | Q9BWF3 | protein_coding | tolerated(0.09) | benign(0.292) | TCGA-D8-A1XQ-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
RBM4 | insertion | Frame_Shift_Ins | novel | c.751_752insT | p.Gln251LeufsTer24 | p.Q251Lfs*24 | Q9BWF3 | protein_coding | TCGA-A8-A0A6-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | epirubicin | CR | ||
RBM4 | insertion | Frame_Shift_Ins | novel | c.753_754insATGTCCTCTTCCCTCTTGCCATCGTG | p.Leu252MetfsTer125 | p.L252Mfs*125 | Q9BWF3 | protein_coding | TCGA-A8-A0A6-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | epirubicin | CR | ||
RBM4 | SNV | Missense_Mutation | rs752990000 | c.721G>A | p.Val241Met | p.V241M | Q9BWF3 | protein_coding | tolerated(0.21) | benign(0.003) | TCGA-C5-A1ML-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | PD |
RBM4 | SNV | Missense_Mutation | c.359G>A | p.Arg120Gln | p.R120Q | Q9BWF3 | protein_coding | tolerated(0.07) | benign(0.124) | TCGA-AA-3811-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | PD | |
RBM4 | SNV | Missense_Mutation | rs765301901 | c.158N>A | p.Arg53His | p.R53H | Q9BWF3 | protein_coding | tolerated(0.1) | benign(0.075) | TCGA-AA-3821-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
RBM4 | SNV | Missense_Mutation | c.245N>C | p.Val82Ala | p.V82A | Q9BWF3 | protein_coding | deleterious(0) | probably_damaging(0.996) | TCGA-AD-6889-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Chemotherapy | xeloda | PD | |
RBM4 | SNV | Missense_Mutation | c.1046N>A | p.Arg349Gln | p.R349Q | Q9BWF3 | protein_coding | deleterious(0.02) | benign(0.174) | TCGA-AZ-6601-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
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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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