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Gene: FER1L6 |
Gene summary for FER1L6 |
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Gene information | Species | Human | Gene symbol | FER1L6 | Gene ID | 654463 |
Gene name | fer-1 like family member 6 | |
Gene Alias | C8ORFK23 | |
Cytomap | 8q24.13 | |
Gene Type | protein-coding | GO ID | GO:0007009 | UniProtAcc | Q2WGJ9 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
654463 | FER1L6 | HTA11_2487_2000001011 | Human | Colorectum | SER | 2.01e-02 | 2.67e-01 | -0.1808 |
654463 | FER1L6 | HTA11_78_2000001011 | Human | Colorectum | AD | 6.28e-05 | 3.49e-01 | -0.1088 |
654463 | FER1L6 | HTA11_411_2000001011 | Human | Colorectum | SER | 6.63e-05 | 9.28e-01 | -0.2602 |
654463 | FER1L6 | HTA11_2112_2000001011 | Human | Colorectum | SER | 3.88e-04 | 9.70e-01 | -0.2196 |
654463 | FER1L6 | Pat02-B | Human | Stomach | GC | 1.08e-13 | 3.34e-01 | 0.0368 |
654463 | FER1L6 | Pat03-B | Human | Stomach | GC | 1.84e-03 | 2.43e-01 | 0.3693 |
654463 | FER1L6 | Pat04-B | Human | Stomach | GC | 1.80e-12 | 3.94e-01 | -0.1483 |
654463 | FER1L6 | Pat05-B | Human | Stomach | GC | 2.01e-02 | 2.30e-01 | -0.0353 |
654463 | FER1L6 | Pat06-B | Human | Stomach | GC | 9.30e-09 | 2.45e-01 | -0.1961 |
654463 | FER1L6 | Pat10-B | Human | Stomach | GC | 2.06e-06 | 4.79e-01 | 0.084 |
654463 | FER1L6 | Pat11-B | Human | Stomach | GC | 3.43e-07 | 2.68e-01 | -0.182 |
654463 | FER1L6 | Pat13-B | Human | Stomach | GC | 1.66e-05 | 3.41e-01 | 0.0555 |
654463 | FER1L6 | Pat15-B | Human | Stomach | GC | 4.46e-06 | 3.13e-01 | -0.0778 |
654463 | FER1L6 | Pat18-B | Human | Stomach | GC | 4.35e-23 | 6.07e-01 | -0.0432 |
654463 | FER1L6 | Pat19-B | Human | Stomach | GC | 2.04e-08 | 3.47e-01 | 0.0826 |
654463 | FER1L6 | Pat22-B | Human | Stomach | GC | 1.24e-16 | 3.94e-01 | -0.1042 |
654463 | FER1L6 | Pat24-B | Human | Stomach | GC | 3.34e-05 | 2.87e-01 | -0.1184 |
654463 | FER1L6 | Pat25-A | Human | Stomach | CAG with IM | 2.85e-11 | 2.25e-01 | -0.1648 |
654463 | FER1L6 | Pat26-A | Human | Stomach | CSG | 4.59e-13 | 2.69e-01 | -0.2402 |
654463 | FER1L6 | Pat28-A | Human | Stomach | CSG | 5.25e-08 | 2.70e-01 | -0.2594 |
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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:0007009 | Colorectum | SER | plasma membrane organization | 36/2897 | 142/18723 | 1.50e-03 | 1.62e-02 | 36 |
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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 |
FER1L6 | SNV | Missense_Mutation | novel | c.3671N>A | p.Ala1224Asp | p.A1224D | Q2WGJ9 | protein_coding | tolerated(0.35) | benign(0.08) | TCGA-AP-A051-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
FER1L6 | SNV | Missense_Mutation | c.1192N>G | p.Leu398Val | p.L398V | Q2WGJ9 | protein_coding | deleterious(0) | benign(0.342) | TCGA-AP-A056-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
FER1L6 | SNV | Missense_Mutation | c.3122N>A | p.Ser1041Asn | p.S1041N | Q2WGJ9 | protein_coding | tolerated(0.48) | benign(0.003) | TCGA-AP-A056-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
FER1L6 | SNV | Missense_Mutation | c.2874N>T | p.Gln958His | p.Q958H | Q2WGJ9 | protein_coding | deleterious(0) | possibly_damaging(0.821) | TCGA-AP-A059-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
FER1L6 | SNV | Missense_Mutation | c.3296N>C | p.Ile1099Thr | p.I1099T | Q2WGJ9 | protein_coding | tolerated(0.55) | benign(0) | TCGA-AP-A059-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
FER1L6 | SNV | Missense_Mutation | c.4754C>A | p.Pro1585His | p.P1585H | Q2WGJ9 | protein_coding | deleterious(0) | probably_damaging(0.987) | TCGA-AP-A1DK-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
FER1L6 | SNV | Missense_Mutation | novel | c.4766C>T | p.Ser1589Phe | p.S1589F | Q2WGJ9 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-AP-A1DV-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
FER1L6 | SNV | Missense_Mutation | novel | c.212N>A | p.Thr71Asn | p.T71N | Q2WGJ9 | protein_coding | tolerated(0.15) | benign(0.109) | TCGA-AP-A1E0-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | paclitaxel | SD |
FER1L6 | SNV | Missense_Mutation | rs370359921 | c.1612N>A | p.Glu538Lys | p.E538K | Q2WGJ9 | protein_coding | tolerated(0.3) | benign(0.036) | TCGA-AP-A1E0-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | paclitaxel | SD |
FER1L6 | SNV | Missense_Mutation | novel | c.2412N>A | p.Met804Ile | p.M804I | Q2WGJ9 | protein_coding | tolerated(0.21) | benign(0) | TCGA-AX-A06F-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | carboplatin | 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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