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Gene: MLXIPL |
Gene summary for MLXIPL |
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Gene information | Species | Human | Gene symbol | MLXIPL | Gene ID | 51085 |
Gene name | MLX interacting protein like | |
Gene Alias | CHREBP | |
Cytomap | 7q11.23 | |
Gene Type | protein-coding | GO ID | GO:0000122 | UniProtAcc | Q9NP71 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
51085 | MLXIPL | HTA11_866_3004761011 | Human | Colorectum | AD | 1.49e-02 | 2.06e-01 | 0.096 |
51085 | MLXIPL | HTA11_99999970781_79442 | Human | Colorectum | MSS | 3.57e-16 | 6.90e-01 | 0.294 |
51085 | MLXIPL | HTA11_99999965104_69814 | Human | Colorectum | MSS | 2.66e-33 | 1.58e+00 | 0.281 |
51085 | MLXIPL | HTA11_99999971662_82457 | Human | Colorectum | MSS | 4.58e-42 | 1.32e+00 | 0.3859 |
51085 | MLXIPL | HTA11_99999974143_84620 | Human | Colorectum | MSS | 1.01e-38 | 9.69e-01 | 0.3005 |
51085 | MLXIPL | A015-C-203 | Human | Colorectum | FAP | 3.44e-04 | 2.95e-01 | -0.1294 |
51085 | MLXIPL | A002-C-021 | Human | Colorectum | FAP | 5.71e-04 | 3.56e-01 | 0.1171 |
51085 | MLXIPL | A015-C-104 | Human | Colorectum | FAP | 4.86e-05 | 2.30e-01 | -0.1899 |
51085 | MLXIPL | A001-C-007 | Human | Colorectum | CRC | 2.85e-08 | 8.17e-01 | 0.1899 |
51085 | MLXIPL | F072B | Human | Colorectum | FAP | 1.38e-03 | 4.63e-01 | 0.257 |
51085 | MLXIPL | CRC-1-8810 | Human | Colorectum | CRC | 1.92e-07 | 5.34e-01 | 0.6257 |
51085 | MLXIPL | NAFLD1 | Human | Liver | NAFLD | 1.46e-10 | 1.16e+00 | -0.04 |
51085 | MLXIPL | S43 | Human | Liver | Cirrhotic | 2.17e-11 | -3.33e-01 | -0.0187 |
51085 | MLXIPL | HCC1_Meng | Human | Liver | HCC | 9.32e-68 | -3.44e-02 | 0.0246 |
51085 | MLXIPL | HCC2_Meng | Human | Liver | HCC | 5.36e-17 | -3.62e-01 | 0.0107 |
51085 | MLXIPL | cirrhotic1 | Human | Liver | Cirrhotic | 1.02e-10 | -3.50e-02 | 0.0202 |
51085 | MLXIPL | cirrhotic2 | Human | Liver | Cirrhotic | 4.18e-09 | -9.91e-02 | 0.0201 |
51085 | MLXIPL | cirrhotic3 | Human | Liver | Cirrhotic | 2.49e-03 | -2.47e-01 | 0.0215 |
51085 | MLXIPL | HCC1 | Human | Liver | HCC | 2.13e-24 | 4.76e+00 | 0.5336 |
51085 | MLXIPL | HCC2 | Human | Liver | HCC | 3.30e-40 | 5.43e+00 | 0.5341 |
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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:000913222 | Liver | HCC | nucleoside diphosphate metabolic process | 81/7958 | 124/18723 | 2.34e-07 | 4.17e-06 | 81 |
GO:000610921 | Liver | HCC | regulation of carbohydrate metabolic process | 109/7958 | 178/18723 | 3.36e-07 | 5.78e-06 | 109 |
GO:004693922 | Liver | HCC | nucleotide phosphorylation | 68/7958 | 101/18723 | 3.95e-07 | 6.70e-06 | 68 |
GO:00550882 | Liver | HCC | lipid homeostasis | 103/7958 | 167/18723 | 4.27e-07 | 7.18e-06 | 103 |
GO:000616522 | Liver | HCC | nucleoside diphosphate phosphorylation | 66/7958 | 99/18723 | 1.01e-06 | 1.52e-05 | 66 |
GO:000609622 | Liver | HCC | glycolytic process | 56/7958 | 81/18723 | 1.11e-06 | 1.65e-05 | 56 |
GO:003428422 | Liver | HCC | response to monosaccharide | 131/7958 | 225/18723 | 1.32e-06 | 1.91e-05 | 131 |
GO:000675722 | Liver | HCC | ATP generation from ADP | 56/7958 | 82/18723 | 2.06e-06 | 2.83e-05 | 56 |
GO:004218021 | Liver | HCC | cellular ketone metabolic process | 123/7958 | 211/18723 | 2.52e-06 | 3.37e-05 | 123 |
GO:00192162 | Liver | HCC | regulation of lipid metabolic process | 181/7958 | 331/18723 | 4.58e-06 | 5.79e-05 | 181 |
GO:000974622 | Liver | HCC | response to hexose | 126/7958 | 219/18723 | 4.81e-06 | 6.06e-05 | 126 |
GO:000974912 | Liver | HCC | response to glucose | 121/7958 | 212/18723 | 1.24e-05 | 1.39e-04 | 121 |
GO:000663321 | Liver | HCC | fatty acid biosynthetic process | 96/7958 | 163/18723 | 1.71e-05 | 1.85e-04 | 96 |
GO:004347021 | Liver | HCC | regulation of carbohydrate catabolic process | 39/7958 | 56/18723 | 3.63e-05 | 3.61e-04 | 39 |
GO:001810511 | Liver | HCC | peptidyl-serine phosphorylation | 169/7958 | 315/18723 | 3.86e-05 | 3.81e-04 | 169 |
GO:190357822 | Liver | HCC | regulation of ATP metabolic process | 55/7958 | 87/18723 | 7.67e-05 | 6.85e-04 | 55 |
GO:000611021 | Liver | HCC | regulation of glycolytic process | 32/7958 | 45/18723 | 9.63e-05 | 8.34e-04 | 32 |
GO:001820911 | Liver | HCC | peptidyl-serine modification | 177/7958 | 338/18723 | 1.45e-04 | 1.17e-03 | 177 |
GO:00468902 | Liver | HCC | regulation of lipid biosynthetic process | 96/7958 | 171/18723 | 2.14e-04 | 1.63e-03 | 96 |
GO:00105652 | Liver | HCC | regulation of cellular ketone metabolic process | 77/7958 | 133/18723 | 2.41e-04 | 1.80e-03 | 77 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa049324 | Colorectum | MSS | Non-alcoholic fatty liver disease | 85/1875 | 155/8465 | 4.19e-19 | 1.17e-17 | 7.17e-18 | 85 |
hsa04931 | Colorectum | MSS | Insulin resistance | 36/1875 | 108/8465 | 4.74e-03 | 2.01e-02 | 1.23e-02 | 36 |
hsa049325 | Colorectum | MSS | Non-alcoholic fatty liver disease | 85/1875 | 155/8465 | 4.19e-19 | 1.17e-17 | 7.17e-18 | 85 |
hsa049311 | Colorectum | MSS | Insulin resistance | 36/1875 | 108/8465 | 4.74e-03 | 2.01e-02 | 1.23e-02 | 36 |
hsa049328 | Colorectum | FAP | Non-alcoholic fatty liver disease | 54/1404 | 155/8465 | 1.98e-08 | 6.20e-07 | 3.77e-07 | 54 |
hsa049312 | Colorectum | FAP | Insulin resistance | 32/1404 | 108/8465 | 4.90e-04 | 3.56e-03 | 2.16e-03 | 32 |
hsa049329 | Colorectum | FAP | Non-alcoholic fatty liver disease | 54/1404 | 155/8465 | 1.98e-08 | 6.20e-07 | 3.77e-07 | 54 |
hsa049313 | Colorectum | FAP | Insulin resistance | 32/1404 | 108/8465 | 4.90e-04 | 3.56e-03 | 2.16e-03 | 32 |
hsa049314 | Colorectum | CRC | Insulin resistance | 28/1091 | 108/8465 | 1.78e-04 | 2.37e-03 | 1.61e-03 | 28 |
hsa049315 | Colorectum | CRC | Insulin resistance | 28/1091 | 108/8465 | 1.78e-04 | 2.37e-03 | 1.61e-03 | 28 |
hsa049316 | Liver | NAFLD | Insulin resistance | 29/1043 | 108/8465 | 3.01e-05 | 7.59e-04 | 6.11e-04 | 29 |
hsa0493214 | Liver | NAFLD | Non-alcoholic fatty liver disease | 33/1043 | 155/8465 | 1.04e-03 | 1.42e-02 | 1.14e-02 | 33 |
hsa0493111 | Liver | NAFLD | Insulin resistance | 29/1043 | 108/8465 | 3.01e-05 | 7.59e-04 | 6.11e-04 | 29 |
hsa0493215 | Liver | NAFLD | Non-alcoholic fatty liver disease | 33/1043 | 155/8465 | 1.04e-03 | 1.42e-02 | 1.14e-02 | 33 |
hsa0493222 | Liver | Cirrhotic | Non-alcoholic fatty liver disease | 106/2530 | 155/8465 | 2.16e-23 | 2.40e-21 | 1.48e-21 | 106 |
hsa0493232 | Liver | Cirrhotic | Non-alcoholic fatty liver disease | 106/2530 | 155/8465 | 2.16e-23 | 2.40e-21 | 1.48e-21 | 106 |
hsa0493242 | Liver | HCC | Non-alcoholic fatty liver disease | 124/4020 | 155/8465 | 4.54e-17 | 2.54e-15 | 1.41e-15 | 124 |
hsa0493121 | Liver | HCC | Insulin resistance | 77/4020 | 108/8465 | 3.89e-07 | 4.46e-06 | 2.48e-06 | 77 |
hsa0493252 | Liver | HCC | Non-alcoholic fatty liver disease | 124/4020 | 155/8465 | 4.54e-17 | 2.54e-15 | 1.41e-15 | 124 |
hsa0493131 | Liver | HCC | Insulin resistance | 77/4020 | 108/8465 | 3.89e-07 | 4.46e-06 | 2.48e-06 | 77 |
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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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∗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 |
MLXIPL | SNV | Missense_Mutation | c.2422N>G | p.Leu808Val | p.L808V | Q9NP71 | protein_coding | deleterious(0) | probably_damaging(0.991) | TCGA-AC-A5XS-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | femara | SD | |
MLXIPL | SNV | Missense_Mutation | novel | c.2437N>T | p.Pro813Ser | p.P813S | Q9NP71 | protein_coding | deleterious(0) | probably_damaging(0.996) | TCGA-BH-A0EA-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | taxotere | CR |
MLXIPL | SNV | Missense_Mutation | novel | c.2033N>A | p.Thr678Lys | p.T678K | Q9NP71 | protein_coding | deleterious(0) | probably_damaging(0.966) | TCGA-UL-AAZ6-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | herceptin | SD |
MLXIPL | SNV | Missense_Mutation | novel | c.962C>T | p.Pro321Leu | p.P321L | Q9NP71 | protein_coding | deleterious(0.02) | benign(0) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
MLXIPL | SNV | Missense_Mutation | rs551026243 | c.1034N>T | p.Ser345Leu | p.S345L | Q9NP71 | protein_coding | tolerated(0.51) | benign(0) | TCGA-C5-A1BQ-01 | Cervix | cervical & endocervical cancer | Female | >=65 | III/IV | Chemotherapy | cisplatin | CR |
MLXIPL | SNV | Missense_Mutation | c.838G>C | p.Asp280His | p.D280H | Q9NP71 | protein_coding | deleterious(0) | probably_damaging(0.993) | TCGA-DR-A0ZM-01 | Cervix | cervical & endocervical cancer | Female | <65 | III/IV | Unspecific | Cisplatin | SD | |
MLXIPL | SNV | Missense_Mutation | rs551026243 | c.1034C>T | p.Ser345Leu | p.S345L | Q9NP71 | protein_coding | tolerated(0.51) | benign(0) | TCGA-AA-3492-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
MLXIPL | SNV | Missense_Mutation | c.199N>C | p.Asp67His | p.D67H | Q9NP71 | protein_coding | tolerated(0.45) | possibly_damaging(0.511) | TCGA-AA-3510-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
MLXIPL | SNV | Missense_Mutation | rs781908299 | c.1916N>A | p.Arg639Gln | p.R639Q | Q9NP71 | protein_coding | tolerated(0.21) | probably_damaging(0.921) | TCGA-AM-5821-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
MLXIPL | SNV | Missense_Mutation | c.1315N>G | p.Thr439Ala | p.T439A | Q9NP71 | protein_coding | tolerated(0.6) | benign(0) | TCGA-AY-6197-01 | Colorectum | colon adenocarcinoma | Male | <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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