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Gene: FCRL5 |
Gene summary for FCRL5 |
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Gene information | Species | Human | Gene symbol | FCRL5 | Gene ID | 83416 |
Gene name | Fc receptor like 5 | |
Gene Alias | BXMAS1 | |
Cytomap | 1q23.1 | |
Gene Type | protein-coding | GO ID | GO:0007154 | UniProtAcc | Q96RD9 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
83416 | FCRL5 | GSM5353218_PA_PB1B_Pool_1_2_S74_L003 | Human | Prostate | Tumor | 2.52e-09 | 8.28e-01 | 0.1479 |
83416 | FCRL5 | GSM5353220_PA_PB1B_Pool_3_S51_L002 | Human | Prostate | Tumor | 2.22e-03 | 5.26e-01 | 0.1531 |
83416 | FCRL5 | GSM5353225_PA_PR5196-1_Pool_1_2_3_S53_L002 | Human | Prostate | Tumor | 3.50e-02 | 4.14e-01 | 0.1619 |
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Tissue | Expression Dynamics | Abbreviation |
Prostate | ![]() | BPH: Benign Prostatic Hyperplasia |
∗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 |
FCRL5 | SNV | Missense_Mutation | rs746634732 | c.679N>T | p.Arg227Cys | p.R227C | Q96RD9 | protein_coding | tolerated(0.19) | benign(0.007) | TCGA-C8-A275-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
FCRL5 | SNV | Missense_Mutation | c.1162G>A | p.Glu388Lys | p.E388K | Q96RD9 | protein_coding | tolerated(0.92) | benign(0.304) | TCGA-D8-A1J8-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | nolvadex | SD | |
FCRL5 | SNV | Missense_Mutation | rs376321602 | c.1694G>C | p.Arg565Pro | p.R565P | Q96RD9 | protein_coding | deleterious(0.02) | possibly_damaging(0.828) | TCGA-D8-A1JK-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
FCRL5 | SNV | Missense_Mutation | c.1516N>G | p.Gln506Glu | p.Q506E | Q96RD9 | protein_coding | deleterious(0.04) | possibly_damaging(0.497) | TCGA-D8-A1Y1-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Hormone Therapy | tamoxiphen | PD | |
FCRL5 | SNV | Missense_Mutation | c.1162N>A | p.Glu388Lys | p.E388K | Q96RD9 | protein_coding | tolerated(0.92) | benign(0.304) | TCGA-D8-A27G-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
FCRL5 | SNV | Missense_Mutation | c.843N>C | p.Gln281His | p.Q281H | Q96RD9 | protein_coding | tolerated(0.06) | probably_damaging(0.932) | TCGA-OL-A5DA-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
FCRL5 | insertion | Frame_Shift_Ins | novel | c.2361dupT | p.His788SerfsTer2 | p.H788Sfs*2 | Q96RD9 | protein_coding | TCGA-BH-A18G-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | ||
FCRL5 | SNV | Missense_Mutation | novel | c.2092G>A | p.Val698Ile | p.V698I | Q96RD9 | protein_coding | tolerated(0.09) | possibly_damaging(0.888) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
FCRL5 | SNV | Missense_Mutation | c.2524N>A | p.Ala842Thr | p.A842T | Q96RD9 | protein_coding | tolerated(0.06) | benign(0.043) | TCGA-C5-A7CL-01 | Cervix | cervical & endocervical cancer | Female | <65 | III/IV | Chemotherapy | cisplatin | PD | |
FCRL5 | SNV | Missense_Mutation | c.1999A>T | p.Arg667Trp | p.R667W | Q96RD9 | protein_coding | deleterious(0) | probably_damaging(0.965) | TCGA-FU-A40J-01 | Cervix | cervical & endocervical cancer | Female | <65 | III/IV | Chemotherapy | carboplatin | CR |
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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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