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Gene: UNC5B |
Gene summary for UNC5B |
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Gene information | Species | Human | Gene symbol | UNC5B | Gene ID | 219699 |
Gene name | unc-5 netrin receptor B | |
Gene Alias | UNC5H2 | |
Cytomap | 10q22.1 | |
Gene Type | protein-coding | GO ID | GO:0000902 | UniProtAcc | Q8IZJ1 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
219699 | UNC5B | HTA11_2487_2000001011 | Human | Colorectum | SER | 1.52e-05 | 3.33e-01 | -0.1808 |
219699 | UNC5B | HTA11_347_2000001011 | Human | Colorectum | AD | 2.66e-09 | 3.80e-01 | -0.1954 |
219699 | UNC5B | HTA11_411_2000001011 | Human | Colorectum | SER | 2.25e-03 | 5.85e-01 | -0.2602 |
219699 | UNC5B | HTA11_3361_2000001011 | Human | Colorectum | AD | 3.34e-08 | 5.00e-01 | -0.1207 |
219699 | UNC5B | HTA11_83_2000001011 | Human | Colorectum | SER | 2.60e-09 | 5.70e-01 | -0.1526 |
219699 | UNC5B | HTA11_696_2000001011 | Human | Colorectum | AD | 3.27e-12 | 4.93e-01 | -0.1464 |
219699 | UNC5B | HTA11_1391_2000001011 | Human | Colorectum | AD | 1.23e-03 | 2.63e-01 | -0.059 |
219699 | UNC5B | HTA11_2992_2000001011 | Human | Colorectum | SER | 5.94e-03 | 5.20e-01 | -0.1706 |
219699 | UNC5B | HTA11_5212_2000001011 | Human | Colorectum | AD | 1.36e-06 | 5.22e-01 | -0.2061 |
219699 | UNC5B | HTA11_546_2000001011 | Human | Colorectum | AD | 8.85e-05 | 4.97e-01 | -0.0842 |
219699 | UNC5B | C04 | Human | Oral cavity | OSCC | 4.76e-05 | 3.23e-01 | 0.2633 |
219699 | UNC5B | C30 | Human | Oral cavity | OSCC | 2.43e-06 | 4.85e-01 | 0.3055 |
219699 | UNC5B | C38 | Human | Oral cavity | OSCC | 1.88e-05 | 8.92e-01 | 0.172 |
219699 | UNC5B | C43 | Human | Oral cavity | OSCC | 4.12e-10 | 2.82e-01 | 0.1704 |
219699 | UNC5B | C51 | Human | Oral cavity | OSCC | 1.88e-03 | 3.68e-01 | 0.2674 |
219699 | UNC5B | C57 | Human | Oral cavity | OSCC | 5.04e-05 | 2.89e-01 | 0.1679 |
219699 | UNC5B | C06 | Human | Oral cavity | OSCC | 9.67e-10 | 1.09e+00 | 0.2699 |
219699 | UNC5B | C08 | Human | Oral cavity | OSCC | 1.93e-02 | 1.52e-01 | 0.1919 |
219699 | UNC5B | C09 | Human | Oral cavity | OSCC | 1.42e-09 | 2.89e-01 | 0.1431 |
219699 | UNC5B | LN38 | Human | Oral cavity | OSCC | 2.79e-09 | 1.19e+00 | 0.168 |
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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:200123720 | Oral cavity | OSCC | negative regulation of extrinsic apoptotic signaling pathway | 60/7305 | 97/18723 | 4.31e-06 | 4.98e-05 | 60 |
GO:004352310 | Oral cavity | OSCC | regulation of neuron apoptotic process | 111/7305 | 212/18723 | 5.12e-05 | 4.27e-04 | 111 |
GO:19012159 | Oral cavity | OSCC | negative regulation of neuron death | 104/7305 | 208/18723 | 7.90e-04 | 4.27e-03 | 104 |
GO:20012393 | Oral cavity | OSCC | regulation of extrinsic apoptotic signaling pathway in absence of ligand | 27/7305 | 43/18723 | 1.35e-03 | 6.62e-03 | 27 |
GO:19010991 | Oral cavity | OSCC | negative regulation of signal transduction in absence of ligand | 20/7305 | 33/18723 | 9.78e-03 | 3.45e-02 | 20 |
GO:20012401 | Oral cavity | OSCC | negative regulation of extrinsic apoptotic signaling pathway in absence of ligand | 20/7305 | 33/18723 | 9.78e-03 | 3.45e-02 | 20 |
GO:006156410 | Oral cavity | OSCC | axon development | 207/7305 | 467/18723 | 1.01e-02 | 3.51e-02 | 207 |
GO:2001233113 | Thyroid | PTC | regulation of apoptotic signaling pathway | 197/5968 | 356/18723 | 2.58e-20 | 3.69e-18 | 197 |
GO:2001234113 | Thyroid | PTC | negative regulation of apoptotic signaling pathway | 124/5968 | 224/18723 | 2.57e-13 | 1.32e-11 | 124 |
GO:0097191113 | Thyroid | PTC | extrinsic apoptotic signaling pathway | 117/5968 | 219/18723 | 2.73e-11 | 1.03e-09 | 117 |
GO:0070997113 | Thyroid | PTC | neuron death | 171/5968 | 361/18723 | 4.32e-10 | 1.38e-08 | 171 |
GO:1901214113 | Thyroid | PTC | regulation of neuron death | 151/5968 | 319/18723 | 4.74e-09 | 1.24e-07 | 151 |
GO:2001236113 | Thyroid | PTC | regulation of extrinsic apoptotic signaling pathway | 82/5968 | 151/18723 | 9.01e-09 | 2.18e-07 | 82 |
GO:0051402112 | Thyroid | PTC | neuron apoptotic process | 118/5968 | 246/18723 | 8.99e-08 | 1.81e-06 | 118 |
GO:006156419 | Thyroid | PTC | axon development | 199/5968 | 467/18723 | 5.27e-07 | 8.53e-06 | 199 |
GO:0043523110 | Thyroid | PTC | regulation of neuron apoptotic process | 102/5968 | 212/18723 | 5.45e-07 | 8.76e-06 | 102 |
GO:000740918 | Thyroid | PTC | axonogenesis | 178/5968 | 418/18723 | 2.17e-06 | 2.91e-05 | 178 |
GO:2001237113 | Thyroid | PTC | negative regulation of extrinsic apoptotic signaling pathway | 51/5968 | 97/18723 | 1.83e-05 | 1.88e-04 | 51 |
GO:190121518 | Thyroid | PTC | negative regulation of neuron death | 95/5968 | 208/18723 | 2.01e-05 | 2.04e-04 | 95 |
GO:00435245 | Thyroid | PTC | negative regulation of neuron apoptotic process | 66/5968 | 145/18723 | 3.88e-04 | 2.61e-03 | 66 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa04360 | Colorectum | AD | Axon guidance | 61/2092 | 182/8465 | 4.36e-03 | 2.17e-02 | 1.38e-02 | 61 |
hsa043601 | Colorectum | AD | Axon guidance | 61/2092 | 182/8465 | 4.36e-03 | 2.17e-02 | 1.38e-02 | 61 |
hsa0436014 | Oral cavity | OSCC | Axon guidance | 97/3704 | 182/8465 | 5.59e-03 | 1.33e-02 | 6.76e-03 | 97 |
hsa0436015 | Oral cavity | OSCC | Axon guidance | 97/3704 | 182/8465 | 5.59e-03 | 1.33e-02 | 6.76e-03 | 97 |
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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 |
UNC5B | SNV | Missense_Mutation | novel | c.358N>A | p.Leu120Ile | p.L120I | Q8IZJ1 | protein_coding | tolerated(0.36) | probably_damaging(0.996) | TCGA-E9-A1RE-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Hormone Therapy | tamoxiphen | SD |
UNC5B | SNV | Missense_Mutation | novel | c.928A>C | p.Lys310Gln | p.K310Q | Q8IZJ1 | protein_coding | deleterious(0.03) | probably_damaging(0.999) | TCGA-HN-A2NL-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cyclophosphamide | SD |
UNC5B | insertion | Frame_Shift_Ins | novel | c.1601_1602insACTGA | p.Gly536ThrfsTer68 | p.G536Tfs*68 | Q8IZJ1 | protein_coding | TCGA-A2-A0CM-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | adriamycin | PD | ||
UNC5B | SNV | Missense_Mutation | rs199873525 | c.676G>A | p.Val226Met | p.V226M | Q8IZJ1 | protein_coding | tolerated(0.17) | possibly_damaging(0.463) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
UNC5B | SNV | Missense_Mutation | rs759839363 | c.812G>A | p.Arg271Gln | p.R271Q | Q8IZJ1 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
UNC5B | SNV | Missense_Mutation | rs139601435 | c.1210C>T | p.Arg404Cys | p.R404C | Q8IZJ1 | protein_coding | deleterious(0.01) | probably_damaging(0.998) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
UNC5B | SNV | Missense_Mutation | novel | c.541C>T | p.Pro181Ser | p.P181S | Q8IZJ1 | protein_coding | deleterious(0.01) | benign(0.23) | TCGA-EA-A3HS-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
UNC5B | SNV | Missense_Mutation | c.169N>T | p.Ala57Ser | p.A57S | Q8IZJ1 | protein_coding | tolerated(0.07) | probably_damaging(0.998) | TCGA-MY-A913-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |
UNC5B | SNV | Missense_Mutation | rs202076199 | c.1540G>A | p.Asp514Asn | p.D514N | Q8IZJ1 | protein_coding | tolerated(0.5) | benign(0.177) | TCGA-A6-2677-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Ancillary | leucovorin | SD |
UNC5B | SNV | Missense_Mutation | novel | c.1349N>A | p.Gly450Asp | p.G450D | Q8IZJ1 | protein_coding | tolerated(0.05) | probably_damaging(1) | TCGA-A6-3809-01 | Colorectum | colon adenocarcinoma | 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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