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Gene: ARPIN |
Gene summary for ARPIN |
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Gene information | Species | Human | Gene symbol | ARPIN | Gene ID | 348110 |
Gene name | actin related protein 2/3 complex inhibitor | |
Gene Alias | C15orf38 | |
Cytomap | 15q26.1 | |
Gene Type | protein-coding | GO ID | GO:0000902 | UniProtAcc | H0YMP5 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
348110 | ARPIN | HTA11_3410_2000001011 | Human | Colorectum | AD | 2.54e-08 | 1.98e-01 | 0.0155 |
348110 | ARPIN | HTA11_2487_2000001011 | Human | Colorectum | SER | 5.80e-07 | 2.41e-01 | -0.1808 |
348110 | ARPIN | HTA11_1938_2000001011 | Human | Colorectum | AD | 4.00e-12 | 3.71e-01 | -0.0811 |
348110 | ARPIN | HTA11_78_2000001011 | Human | Colorectum | AD | 2.35e-06 | 2.20e-01 | -0.1088 |
348110 | ARPIN | HTA11_347_2000001011 | Human | Colorectum | AD | 2.88e-22 | 4.11e-01 | -0.1954 |
348110 | ARPIN | HTA11_411_2000001011 | Human | Colorectum | SER | 1.20e-07 | 5.38e-01 | -0.2602 |
348110 | ARPIN | HTA11_3361_2000001011 | Human | Colorectum | AD | 1.91e-05 | 2.02e-01 | -0.1207 |
348110 | ARPIN | HTA11_83_2000001011 | Human | Colorectum | SER | 3.64e-05 | 2.45e-01 | -0.1526 |
348110 | ARPIN | HTA11_696_2000001011 | Human | Colorectum | AD | 8.94e-11 | 2.47e-01 | -0.1464 |
348110 | ARPIN | HTA11_866_2000001011 | Human | Colorectum | AD | 1.42e-14 | 3.04e-01 | -0.1001 |
348110 | ARPIN | HTA11_1391_2000001011 | Human | Colorectum | AD | 2.92e-14 | 3.49e-01 | -0.059 |
348110 | ARPIN | HTA11_2992_2000001011 | Human | Colorectum | SER | 1.51e-04 | 3.33e-01 | -0.1706 |
348110 | ARPIN | HTA11_5212_2000001011 | Human | Colorectum | AD | 1.91e-11 | 4.59e-01 | -0.2061 |
348110 | ARPIN | HTA11_5216_2000001011 | Human | Colorectum | SER | 3.40e-02 | 2.22e-01 | -0.1462 |
348110 | ARPIN | HTA11_546_2000001011 | Human | Colorectum | AD | 2.76e-14 | 4.15e-01 | -0.0842 |
348110 | ARPIN | HTA11_7862_2000001011 | Human | Colorectum | AD | 1.12e-06 | 3.55e-01 | -0.0179 |
348110 | ARPIN | HTA11_866_3004761011 | Human | Colorectum | AD | 3.40e-12 | 2.77e-01 | 0.096 |
348110 | ARPIN | HTA11_4255_2000001011 | Human | Colorectum | SER | 3.40e-03 | 3.08e-01 | 0.0446 |
348110 | ARPIN | HTA11_7663_2000001011 | Human | Colorectum | SER | 7.58e-09 | 4.76e-01 | 0.0131 |
348110 | ARPIN | HTA11_10623_2000001011 | Human | Colorectum | AD | 4.46e-06 | 2.81e-01 | -0.0177 |
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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:00019596 | Thyroid | PTC | regulation of cytokine-mediated signaling pathway | 64/5968 | 150/18723 | 3.43e-03 | 1.66e-02 | 64 |
GO:003320916 | Thyroid | PTC | tumor necrosis factor-mediated signaling pathway | 44/5968 | 99/18723 | 5.77e-03 | 2.60e-02 | 44 |
GO:001049832 | Thyroid | ATC | proteasomal protein catabolic process | 309/6293 | 490/18723 | 1.78e-41 | 1.13e-37 | 309 |
GO:0043161210 | Thyroid | ATC | proteasome-mediated ubiquitin-dependent protein catabolic process | 265/6293 | 412/18723 | 7.09e-38 | 1.49e-34 | 265 |
GO:002241124 | Thyroid | ATC | cellular component disassembly | 248/6293 | 443/18723 | 1.34e-22 | 3.69e-20 | 248 |
GO:0000209110 | Thyroid | ATC | protein polyubiquitination | 134/6293 | 236/18723 | 1.86e-13 | 9.20e-12 | 134 |
GO:0043123111 | Thyroid | ATC | positive regulation of I-kappaB kinase/NF-kappaB signaling | 97/6293 | 186/18723 | 1.31e-07 | 2.16e-06 | 97 |
GO:0043122112 | Thyroid | ATC | regulation of I-kappaB kinase/NF-kappaB signaling | 123/6293 | 249/18723 | 1.65e-07 | 2.64e-06 | 123 |
GO:0007249111 | Thyroid | ATC | I-kappaB kinase/NF-kappaB signaling | 135/6293 | 281/18723 | 3.31e-07 | 4.91e-06 | 135 |
GO:003461228 | Thyroid | ATC | response to tumor necrosis factor | 116/6293 | 253/18723 | 3.22e-05 | 2.68e-04 | 116 |
GO:006075912 | Thyroid | ATC | regulation of response to cytokine stimulus | 76/6293 | 162/18723 | 2.92e-04 | 1.85e-03 | 76 |
GO:000195912 | Thyroid | ATC | regulation of cytokine-mediated signaling pathway | 71/6293 | 150/18723 | 3.28e-04 | 2.04e-03 | 71 |
GO:007135627 | Thyroid | ATC | cellular response to tumor necrosis factor | 102/6293 | 229/18723 | 3.52e-04 | 2.18e-03 | 102 |
GO:003320917 | Thyroid | ATC | tumor necrosis factor-mediated signaling pathway | 48/6293 | 99/18723 | 1.51e-03 | 7.70e-03 | 48 |
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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 |
ARPIN | SNV | Missense_Mutation | c.655G>A | p.Ala219Thr | p.A219T | Q7Z6K5 | protein_coding | deleterious(0.02) | probably_damaging(0.961) | TCGA-A1-A0SO-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | SD | ||
ARPIN | SNV | Missense_Mutation | c.134N>T | p.Ser45Phe | p.S45F | Q7Z6K5 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-GM-A2DO-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | tamoxiphen | CR | |
ARPIN | deletion | Frame_Shift_Del | novel | c.608delN | p.Lys203SerfsTer38 | p.K203Sfs*38 | Q7Z6K5 | protein_coding | TCGA-D8-A27V-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | tamoxiphen | SD | ||
ARPIN | SNV | Missense_Mutation | c.143G>A | p.Ser48Asn | p.S48N | Q7Z6K5 | protein_coding | tolerated(0.33) | benign(0.01) | TCGA-AA-3864-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
ARPIN | SNV | Missense_Mutation | rs201638212 | c.416N>T | p.Ala139Val | p.A139V | Q7Z6K5 | protein_coding | deleterious(0.01) | probably_damaging(0.999) | TCGA-AG-A002-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
ARPIN | SNV | Missense_Mutation | novel | c.505N>A | p.Leu169Met | p.L169M | Q7Z6K5 | protein_coding | deleterious(0) | possibly_damaging(0.682) | TCGA-AJ-A3EK-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Chemotherapy | carboplatin | CR |
ARPIN | SNV | Missense_Mutation | rs370605817 | c.212G>A | p.Arg71His | p.R71H | Q7Z6K5 | protein_coding | deleterious(0.04) | benign(0.015) | TCGA-AP-A051-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
ARPIN | SNV | Missense_Mutation | novel | c.127N>A | p.Asp43Asn | p.D43N | Q7Z6K5 | protein_coding | deleterious(0.03) | probably_damaging(0.999) | TCGA-AP-A1DV-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
ARPIN | SNV | Missense_Mutation | c.614N>T | p.Ser205Leu | p.S205L | Q7Z6K5 | protein_coding | tolerated(0.13) | benign(0.003) | TCGA-B5-A0JY-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | doxorubicin | SD | |
ARPIN | SNV | Missense_Mutation | rs749897855 | c.215N>A | p.Arg72His | p.R72H | Q7Z6K5 | protein_coding | deleterious(0) | probably_damaging(0.975) | TCGA-B5-A3FC-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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