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Gene: FNBP1L |
Gene summary for FNBP1L |
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Gene information | Species | Human | Gene symbol | FNBP1L | Gene ID | 54874 |
Gene name | formin binding protein 1 like | |
Gene Alias | C1orf39 | |
Cytomap | 1p22.1 | |
Gene Type | protein-coding | GO ID | GO:0006810 | UniProtAcc | Q5T0N5 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
54874 | FNBP1L | CA_HPV_1 | Human | Cervix | CC | 5.67e-05 | -1.46e-01 | 0.0264 |
54874 | FNBP1L | CCI_2 | Human | Cervix | CC | 4.98e-03 | 8.25e-01 | 0.5249 |
54874 | FNBP1L | CCI_3 | Human | Cervix | CC | 3.87e-07 | 8.26e-01 | 0.516 |
54874 | FNBP1L | H2 | Human | Cervix | HSIL_HPV | 4.87e-08 | 4.25e-01 | 0.0632 |
54874 | FNBP1L | HTA11_3410_2000001011 | Human | Colorectum | AD | 2.36e-30 | -7.36e-01 | 0.0155 |
54874 | FNBP1L | HTA11_2487_2000001011 | Human | Colorectum | SER | 5.08e-11 | -6.56e-01 | -0.1808 |
54874 | FNBP1L | HTA11_2951_2000001011 | Human | Colorectum | AD | 1.83e-03 | -7.07e-01 | 0.0216 |
54874 | FNBP1L | HTA11_1938_2000001011 | Human | Colorectum | AD | 3.32e-04 | -3.28e-01 | -0.0811 |
54874 | FNBP1L | HTA11_3361_2000001011 | Human | Colorectum | AD | 3.47e-11 | -7.79e-01 | -0.1207 |
54874 | FNBP1L | HTA11_83_2000001011 | Human | Colorectum | SER | 1.70e-02 | -4.26e-01 | -0.1526 |
54874 | FNBP1L | HTA11_696_2000001011 | Human | Colorectum | AD | 2.18e-12 | -4.92e-01 | -0.1464 |
54874 | FNBP1L | HTA11_866_2000001011 | Human | Colorectum | AD | 7.08e-06 | -4.25e-01 | -0.1001 |
54874 | FNBP1L | HTA11_2992_2000001011 | Human | Colorectum | SER | 1.01e-04 | -7.53e-01 | -0.1706 |
54874 | FNBP1L | HTA11_5212_2000001011 | Human | Colorectum | AD | 2.01e-05 | -7.95e-01 | -0.2061 |
54874 | FNBP1L | HTA11_5216_2000001011 | Human | Colorectum | SER | 1.40e-05 | -6.58e-01 | -0.1462 |
54874 | FNBP1L | HTA11_9341_2000001011 | Human | Colorectum | SER | 4.01e-05 | -9.03e-01 | -0.00410000000000005 |
54874 | FNBP1L | HTA11_7862_2000001011 | Human | Colorectum | AD | 4.10e-09 | -7.61e-01 | -0.0179 |
54874 | FNBP1L | HTA11_866_3004761011 | Human | Colorectum | AD | 1.14e-19 | -7.20e-01 | 0.096 |
54874 | FNBP1L | HTA11_4255_2000001011 | Human | Colorectum | SER | 2.29e-03 | -6.12e-01 | 0.0446 |
54874 | FNBP1L | HTA11_9408_2000001011 | Human | Colorectum | AD | 8.31e-04 | -9.27e-01 | 0.0451 |
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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 |
GO:003004815 | Prostate | Tumor | actin filament-based movement | 36/3246 | 127/18723 | 1.38e-03 | 8.62e-03 | 36 |
GO:009951514 | Prostate | Tumor | actin filament-based transport | 9/3246 | 21/18723 | 5.54e-03 | 2.61e-02 | 9 |
GO:00070093 | Prostate | Tumor | plasma membrane organization | 36/3246 | 142/18723 | 1.00e-02 | 4.20e-02 | 36 |
GO:009951811 | Prostate | Tumor | vesicle cytoskeletal trafficking | 21/3246 | 73/18723 | 1.06e-02 | 4.41e-02 | 21 |
GO:005165618 | Skin | AK | establishment of organelle localization | 69/1910 | 390/18723 | 3.69e-06 | 9.11e-05 | 69 |
GO:003070519 | Skin | AK | cytoskeleton-dependent intracellular transport | 40/1910 | 195/18723 | 1.29e-05 | 2.58e-04 | 40 |
GO:003134617 | Skin | AK | positive regulation of cell projection organization | 60/1910 | 353/18723 | 5.24e-05 | 8.10e-04 | 60 |
GO:003004816 | Skin | AK | actin filament-based movement | 26/1910 | 127/18723 | 4.11e-04 | 3.93e-03 | 26 |
GO:009951515 | Skin | AK | actin filament-based transport | 8/1910 | 21/18723 | 6.95e-04 | 5.94e-03 | 8 |
GO:012003219 | Skin | AK | regulation of plasma membrane bounded cell projection assembly | 33/1910 | 186/18723 | 1.13e-03 | 8.75e-03 | 33 |
GO:006049119 | Skin | AK | regulation of cell projection assembly | 33/1910 | 188/18723 | 1.36e-03 | 1.01e-02 | 33 |
GO:00300509 | Skin | AK | vesicle transport along actin filament | 7/1910 | 19/18723 | 1.89e-03 | 1.29e-02 | 7 |
GO:005165017 | Skin | AK | establishment of vesicle localization | 28/1910 | 161/18723 | 3.44e-03 | 2.09e-02 | 28 |
GO:001605010 | Skin | AK | vesicle organization | 45/1910 | 300/18723 | 5.44e-03 | 3.02e-02 | 45 |
GO:00995186 | Skin | AK | vesicle cytoskeletal trafficking | 15/1910 | 73/18723 | 6.21e-03 | 3.33e-02 | 15 |
GO:000690024 | Skin | AK | vesicle budding from membrane | 13/1910 | 61/18723 | 7.64e-03 | 3.88e-02 | 13 |
GO:01200348 | Skin | AK | positive regulation of plasma membrane bounded cell projection assembly | 19/1910 | 105/18723 | 9.43e-03 | 4.60e-02 | 19 |
GO:009951516 | Skin | SCCIS | actin filament-based transport | 6/919 | 21/18723 | 3.95e-04 | 6.58e-03 | 6 |
GO:005165619 | Skin | SCCIS | establishment of organelle localization | 34/919 | 390/18723 | 8.85e-04 | 1.15e-02 | 34 |
GO:0030705110 | Skin | SCCIS | cytoskeleton-dependent intracellular transport | 20/919 | 195/18723 | 1.50e-03 | 1.69e-02 | 20 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0513120 | Cervix | CC | Shigellosis | 69/1267 | 247/8465 | 7.64e-08 | 1.03e-06 | 6.10e-07 | 69 |
hsa05131110 | Cervix | CC | Shigellosis | 69/1267 | 247/8465 | 7.64e-08 | 1.03e-06 | 6.10e-07 | 69 |
hsa0513125 | Cervix | HSIL_HPV | Shigellosis | 27/459 | 247/8465 | 3.78e-04 | 3.49e-03 | 2.82e-03 | 27 |
hsa0513135 | Cervix | HSIL_HPV | Shigellosis | 27/459 | 247/8465 | 3.78e-04 | 3.49e-03 | 2.82e-03 | 27 |
hsa05131 | Colorectum | AD | Shigellosis | 109/2092 | 247/8465 | 1.09e-11 | 2.44e-10 | 1.55e-10 | 109 |
hsa051311 | Colorectum | AD | Shigellosis | 109/2092 | 247/8465 | 1.09e-11 | 2.44e-10 | 1.55e-10 | 109 |
hsa051312 | Colorectum | SER | Shigellosis | 87/1580 | 247/8465 | 3.07e-10 | 7.27e-09 | 5.28e-09 | 87 |
hsa051313 | Colorectum | SER | Shigellosis | 87/1580 | 247/8465 | 3.07e-10 | 7.27e-09 | 5.28e-09 | 87 |
hsa051314 | Colorectum | MSS | Shigellosis | 94/1875 | 247/8465 | 6.82e-09 | 1.34e-07 | 8.23e-08 | 94 |
hsa051315 | Colorectum | MSS | Shigellosis | 94/1875 | 247/8465 | 6.82e-09 | 1.34e-07 | 8.23e-08 | 94 |
hsa051318 | Colorectum | FAP | Shigellosis | 76/1404 | 247/8465 | 1.57e-08 | 5.84e-07 | 3.55e-07 | 76 |
hsa051319 | Colorectum | FAP | Shigellosis | 76/1404 | 247/8465 | 1.57e-08 | 5.84e-07 | 3.55e-07 | 76 |
hsa0513110 | Colorectum | CRC | Shigellosis | 59/1091 | 247/8465 | 1.19e-06 | 5.41e-05 | 3.66e-05 | 59 |
hsa0513111 | Colorectum | CRC | Shigellosis | 59/1091 | 247/8465 | 1.19e-06 | 5.41e-05 | 3.66e-05 | 59 |
hsa0513126 | Endometrium | AEH | Shigellosis | 78/1197 | 247/8465 | 9.23e-13 | 2.00e-11 | 1.46e-11 | 78 |
hsa05131111 | Endometrium | AEH | Shigellosis | 78/1197 | 247/8465 | 9.23e-13 | 2.00e-11 | 1.46e-11 | 78 |
hsa0513127 | Endometrium | EEC | Shigellosis | 79/1237 | 247/8465 | 1.80e-12 | 3.95e-11 | 2.95e-11 | 79 |
hsa0513136 | Endometrium | EEC | Shigellosis | 79/1237 | 247/8465 | 1.80e-12 | 3.95e-11 | 2.95e-11 | 79 |
hsa05131211 | Esophagus | ESCC | Shigellosis | 176/4205 | 247/8465 | 2.27e-12 | 4.01e-11 | 2.05e-11 | 176 |
hsa05131310 | Esophagus | ESCC | Shigellosis | 176/4205 | 247/8465 | 2.27e-12 | 4.01e-11 | 2.05e-11 | 176 |
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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 |
FNBP1L | SNV | Missense_Mutation | c.390N>C | p.Trp130Cys | p.W130C | Q5T0N5 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-A2-A0YK-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cytoxan | SD | |
FNBP1L | SNV | Missense_Mutation | c.1171N>A | p.Ala391Thr | p.A391T | Q5T0N5 | protein_coding | tolerated(0.56) | probably_damaging(0.997) | TCGA-A8-A09Z-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
FNBP1L | SNV | Missense_Mutation | rs769227073 | c.1783G>A | p.Asp595Asn | p.D595N | Q5T0N5 | protein_coding | deleterious(0.02) | probably_damaging(0.997) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
FNBP1L | SNV | Missense_Mutation | c.753G>C | p.Met251Ile | p.M251I | Q5T0N5 | protein_coding | tolerated(0.61) | possibly_damaging(0.782) | TCGA-C8-A26Y-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
FNBP1L | SNV | Missense_Mutation | c.287G>T | p.Arg96Ile | p.R96I | Q5T0N5 | protein_coding | deleterious(0.04) | probably_damaging(0.99) | TCGA-C5-A3HE-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | PD | |
FNBP1L | SNV | Missense_Mutation | novel | c.1168N>A | p.Pro390Thr | p.P390T | Q5T0N5 | protein_coding | tolerated(0.18) | benign(0.005) | TCGA-AA-3845-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
FNBP1L | SNV | Missense_Mutation | c.824N>G | p.Phe275Cys | p.F275C | Q5T0N5 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-CA-6718-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | PD | |
FNBP1L | SNV | Missense_Mutation | c.14C>T | p.Thr5Met | p.T5M | Q5T0N5 | protein_coding | deleterious(0) | benign(0.035) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
FNBP1L | SNV | Missense_Mutation | c.1381N>A | p.Leu461Ile | p.L461I | Q5T0N5 | protein_coding | deleterious(0) | probably_damaging(0.977) | TCGA-CK-5916-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
FNBP1L | SNV | Missense_Mutation | novel | c.397A>G | p.Met133Val | p.M133V | Q5T0N5 | protein_coding | deleterious(0) | possibly_damaging(0.841) | TCGA-AG-3732-01 | Colorectum | rectum adenocarcinoma | Female | >=65 | I/II | Chemotherapy | capecitabine | 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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