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Gene: XKR6 |
Gene summary for XKR6 |
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Gene information | Species | Human | Gene symbol | XKR6 | Gene ID | 286046 |
Gene name | XK related 6 | |
Gene Alias | C8orf21 | |
Cytomap | 8p23.1 | |
Gene Type | protein-coding | GO ID | GO:0006810 | UniProtAcc | Q5GH73 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
286046 | XKR6 | CCI_1 | Human | Cervix | CC | 3.26e-11 | 8.41e-01 | 0.528 |
286046 | XKR6 | CCI_2 | Human | Cervix | CC | 1.07e-07 | 7.68e-01 | 0.5249 |
286046 | XKR6 | CCI_3 | Human | Cervix | CC | 4.28e-18 | 7.93e-01 | 0.516 |
286046 | XKR6 | HTA11_3410_2000001011 | Human | Colorectum | AD | 2.83e-17 | -6.05e-01 | 0.0155 |
286046 | XKR6 | HTA11_1938_2000001011 | Human | Colorectum | AD | 3.55e-02 | -3.71e-01 | -0.0811 |
286046 | XKR6 | HTA11_78_2000001011 | Human | Colorectum | AD | 7.77e-07 | -5.68e-01 | -0.1088 |
286046 | XKR6 | HTA11_83_2000001011 | Human | Colorectum | SER | 2.11e-04 | -6.12e-01 | -0.1526 |
286046 | XKR6 | HTA11_866_2000001011 | Human | Colorectum | AD | 1.45e-04 | -3.77e-01 | -0.1001 |
286046 | XKR6 | HTA11_1391_2000001011 | Human | Colorectum | AD | 1.73e-18 | -7.06e-01 | -0.059 |
286046 | XKR6 | HTA11_546_2000001011 | Human | Colorectum | AD | 6.10e-06 | -6.51e-01 | -0.0842 |
286046 | XKR6 | HTA11_7862_2000001011 | Human | Colorectum | AD | 3.36e-04 | -5.15e-01 | -0.0179 |
286046 | XKR6 | HTA11_866_3004761011 | Human | Colorectum | AD | 4.23e-15 | -6.49e-01 | 0.096 |
286046 | XKR6 | HTA11_8622_2000001021 | Human | Colorectum | SER | 3.47e-03 | -5.36e-01 | 0.0528 |
286046 | XKR6 | HTA11_10623_2000001011 | Human | Colorectum | AD | 2.03e-02 | -6.16e-01 | -0.0177 |
286046 | XKR6 | HTA11_10711_2000001011 | Human | Colorectum | AD | 5.68e-07 | -6.10e-01 | 0.0338 |
286046 | XKR6 | HTA11_7696_3000711011 | Human | Colorectum | AD | 2.71e-05 | -4.65e-01 | 0.0674 |
286046 | XKR6 | HTA11_6818_2000001011 | Human | Colorectum | AD | 4.75e-02 | -6.02e-01 | 0.0112 |
286046 | XKR6 | HTA11_6818_2000001021 | Human | Colorectum | AD | 2.20e-11 | -7.62e-01 | 0.0588 |
286046 | XKR6 | HTA11_99999970781_79442 | Human | Colorectum | MSS | 1.97e-29 | -7.49e-01 | 0.294 |
286046 | XKR6 | HTA11_99999965104_69814 | Human | Colorectum | MSS | 2.35e-02 | -5.14e-01 | 0.281 |
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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:0006909 | Cervix | CC | phagocytosis | 53/2311 | 308/18723 | 7.49e-03 | 4.01e-02 | 53 |
GO:00070092 | Cervix | CC | plasma membrane organization | 28/2311 | 142/18723 | 7.85e-03 | 4.14e-02 | 28 |
GO:00103243 | Cervix | CC | membrane invagination | 28/2311 | 144/18723 | 9.50e-03 | 4.72e-02 | 28 |
GO:0010876 | Colorectum | AD | lipid localization | 120/3918 | 448/18723 | 1.59e-03 | 1.33e-02 | 120 |
GO:0006869 | Colorectum | AD | lipid transport | 108/3918 | 398/18723 | 1.67e-03 | 1.39e-02 | 108 |
GO:0015748 | Colorectum | AD | organophosphate ester transport | 42/3918 | 140/18723 | 7.04e-03 | 4.31e-02 | 42 |
GO:0007009 | Colorectum | SER | plasma membrane organization | 36/2897 | 142/18723 | 1.50e-03 | 1.62e-02 | 36 |
GO:00108761 | Colorectum | MSS | lipid localization | 104/3467 | 448/18723 | 6.76e-03 | 4.38e-02 | 104 |
GO:00068691 | Colorectum | FAP | lipid transport | 81/2622 | 398/18723 | 2.84e-04 | 3.76e-03 | 81 |
GO:00108762 | Colorectum | FAP | lipid localization | 85/2622 | 448/18723 | 1.92e-03 | 1.63e-02 | 85 |
GO:0015914 | Colorectum | FAP | phospholipid transport | 23/2622 | 96/18723 | 6.09e-03 | 3.82e-02 | 23 |
GO:00070091 | Colorectum | FAP | plasma membrane organization | 31/2622 | 142/18723 | 7.20e-03 | 4.38e-02 | 31 |
GO:00068692 | Colorectum | CRC | lipid transport | 63/2078 | 398/18723 | 2.36e-03 | 2.26e-02 | 63 |
GO:00108763 | Colorectum | CRC | lipid localization | 68/2078 | 448/18723 | 4.60e-03 | 3.58e-02 | 68 |
GO:00159142 | Lung | IAC | phospholipid transport | 20/2061 | 96/18723 | 3.58e-03 | 3.00e-02 | 20 |
GO:00157482 | Lung | IAC | organophosphate ester transport | 26/2061 | 140/18723 | 5.22e-03 | 3.97e-02 | 26 |
GO:001591411 | Lung | AIS | phospholipid transport | 18/1849 | 96/18723 | 5.64e-03 | 4.76e-02 | 18 |
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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 |
XKR6 | SNV | Missense_Mutation | c.1697G>T | p.Arg566Ile | p.R566I | Q5GH73 | protein_coding | deleterious(0) | probably_damaging(0.991) | TCGA-QG-A5YX-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | xeloda | CR | |
XKR6 | SNV | Missense_Mutation | rs200086321 | c.1664N>T | p.Thr555Met | p.T555M | Q5GH73 | protein_coding | tolerated(0.15) | benign(0.007) | TCGA-A5-A0GH-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
XKR6 | SNV | Missense_Mutation | rs201821196 | c.1727N>A | p.Arg576His | p.R576H | Q5GH73 | protein_coding | tolerated(0.08) | possibly_damaging(0.534) | TCGA-A5-A0GI-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
XKR6 | SNV | Missense_Mutation | rs775809618 | c.1511G>A | p.Arg504Gln | p.R504Q | Q5GH73 | protein_coding | tolerated(0.21) | benign(0.06) | TCGA-A5-A1OF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
XKR6 | SNV | Missense_Mutation | rs202021089 | c.1310N>A | p.Arg437Gln | p.R437Q | Q5GH73 | protein_coding | deleterious(0.01) | probably_damaging(0.994) | TCGA-AJ-A3BG-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Chemotherapy | carboplatin | PD |
XKR6 | SNV | Missense_Mutation | c.1450N>G | p.Phe484Val | p.F484V | Q5GH73 | protein_coding | deleterious(0) | probably_damaging(0.992) | TCGA-AP-A0LM-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | cisplatin | SD | |
XKR6 | SNV | Missense_Mutation | rs374654242 | c.805N>T | p.Arg269Trp | p.R269W | Q5GH73 | protein_coding | deleterious(0.02) | possibly_damaging(0.745) | TCGA-AP-A0LM-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | cisplatin | SD |
XKR6 | SNV | Missense_Mutation | rs761510924 | c.949G>A | p.Glu317Lys | p.E317K | Q5GH73 | protein_coding | tolerated(0.16) | probably_damaging(0.93) | TCGA-AP-A1DM-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
XKR6 | SNV | Missense_Mutation | rs772883147 | c.824N>A | p.Arg275His | p.R275H | Q5GH73 | protein_coding | tolerated(0.11) | probably_damaging(0.98) | TCGA-AX-A06F-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | carboplatin | SD |
XKR6 | SNV | Missense_Mutation | novel | c.421G>A | p.Gly141Arg | p.G141R | Q5GH73 | protein_coding | tolerated(0.07) | possibly_damaging(0.845) | TCGA-AX-A2HD-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | III/IV | 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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