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Gene: MCU |
Gene summary for MCU |
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Gene information | Species | Human | Gene symbol | MCU | Gene ID | 90550 |
Gene name | mitochondrial calcium uniporter | |
Gene Alias | C10orf42 | |
Cytomap | 10q22.1 | |
Gene Type | protein-coding | GO ID | GO:0000266 | UniProtAcc | Q8NE86 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
90550 | MCU | CCI_1 | Human | Cervix | CC | 8.85e-14 | 1.09e+00 | 0.528 |
90550 | MCU | CCI_2 | Human | Cervix | CC | 2.73e-08 | 8.07e-01 | 0.5249 |
90550 | MCU | CCI_3 | Human | Cervix | CC | 2.83e-08 | 5.44e-01 | 0.516 |
90550 | MCU | HTA11_3410_2000001011 | Human | Colorectum | AD | 1.98e-33 | -8.79e-01 | 0.0155 |
90550 | MCU | HTA11_2951_2000001011 | Human | Colorectum | AD | 9.76e-04 | -8.53e-01 | 0.0216 |
90550 | MCU | HTA11_347_2000001011 | Human | Colorectum | AD | 6.87e-15 | 6.61e-01 | -0.1954 |
90550 | MCU | HTA11_3361_2000001011 | Human | Colorectum | AD | 7.02e-03 | -4.41e-01 | -0.1207 |
90550 | MCU | HTA11_866_3004761011 | Human | Colorectum | AD | 1.66e-09 | -6.12e-01 | 0.096 |
90550 | MCU | HTA11_8622_2000001021 | Human | Colorectum | SER | 4.25e-07 | -7.33e-01 | 0.0528 |
90550 | MCU | HTA11_7696_3000711011 | Human | Colorectum | AD | 1.41e-07 | -4.49e-01 | 0.0674 |
90550 | MCU | HTA11_6818_2000001011 | Human | Colorectum | AD | 2.38e-03 | -4.77e-01 | 0.0112 |
90550 | MCU | HTA11_99999970781_79442 | Human | Colorectum | MSS | 1.22e-18 | -5.64e-01 | 0.294 |
90550 | MCU | HTA11_99999971662_82457 | Human | Colorectum | MSS | 6.16e-12 | -5.87e-01 | 0.3859 |
90550 | MCU | HTA11_99999973899_84307 | Human | Colorectum | MSS | 2.22e-11 | -9.20e-01 | 0.2585 |
90550 | MCU | HTA11_99999974143_84620 | Human | Colorectum | MSS | 6.44e-53 | -1.12e+00 | 0.3005 |
90550 | MCU | F007 | Human | Colorectum | FAP | 3.20e-02 | -4.44e-01 | 0.1176 |
90550 | MCU | A001-C-207 | Human | Colorectum | FAP | 1.38e-04 | -4.64e-01 | 0.1278 |
90550 | MCU | A015-C-203 | Human | Colorectum | FAP | 7.03e-28 | -5.67e-01 | -0.1294 |
90550 | MCU | A015-C-204 | Human | Colorectum | FAP | 1.28e-07 | -4.91e-01 | -0.0228 |
90550 | MCU | A014-C-040 | Human | Colorectum | FAP | 2.32e-10 | -8.95e-01 | -0.1184 |
Page: 1 2 3 4 5 6 7 8 9 10 |
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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:19049516 | Stomach | GC | positive regulation of establishment of protein localization | 39/1159 | 319/18723 | 3.79e-05 | 9.76e-04 | 39 |
GO:0097530 | Stomach | GC | granulocyte migration | 23/1159 | 148/18723 | 3.99e-05 | 1.00e-03 | 23 |
GO:00716925 | Stomach | GC | protein localization to extracellular region | 43/1159 | 368/18723 | 4.61e-05 | 1.11e-03 | 43 |
GO:00093065 | Stomach | GC | protein secretion | 42/1159 | 359/18723 | 5.46e-05 | 1.29e-03 | 42 |
GO:0030593 | Stomach | GC | neutrophil chemotaxis | 18/1159 | 103/18723 | 5.67e-05 | 1.31e-03 | 18 |
GO:00355925 | Stomach | GC | establishment of protein localization to extracellular region | 42/1159 | 360/18723 | 5.82e-05 | 1.34e-03 | 42 |
GO:00108215 | Stomach | GC | regulation of mitochondrion organization | 22/1159 | 144/18723 | 7.57e-05 | 1.64e-03 | 22 |
GO:0097529 | Stomach | GC | myeloid leukocyte migration | 29/1159 | 220/18723 | 9.69e-05 | 1.97e-03 | 29 |
GO:0002685 | Stomach | GC | regulation of leukocyte migration | 28/1159 | 210/18723 | 1.04e-04 | 2.05e-03 | 28 |
GO:00507146 | Stomach | GC | positive regulation of protein secretion | 21/1159 | 137/18723 | 1.04e-04 | 2.05e-03 | 21 |
GO:00507085 | Stomach | GC | regulation of protein secretion | 33/1159 | 268/18723 | 1.27e-04 | 2.40e-03 | 33 |
GO:00512226 | Stomach | GC | positive regulation of protein transport | 36/1159 | 303/18723 | 1.33e-04 | 2.49e-03 | 36 |
GO:1990266 | Stomach | GC | neutrophil migration | 19/1159 | 122/18723 | 1.77e-04 | 3.08e-03 | 19 |
GO:00158335 | Stomach | GC | peptide transport | 32/1159 | 264/18723 | 2.13e-04 | 3.61e-03 | 32 |
GO:0060326 | Stomach | GC | cell chemotaxis | 35/1159 | 310/18723 | 4.34e-04 | 6.46e-03 | 35 |
GO:00428863 | Stomach | GC | amide transport | 34/1159 | 301/18723 | 5.16e-04 | 7.28e-03 | 34 |
GO:0002687 | Stomach | GC | positive regulation of leukocyte migration | 19/1159 | 135/18723 | 6.56e-04 | 8.76e-03 | 19 |
GO:00320244 | Stomach | GC | positive regulation of insulin secretion | 13/1159 | 78/18723 | 9.38e-04 | 1.14e-02 | 13 |
GO:0071622 | Stomach | GC | regulation of granulocyte chemotaxis | 10/1159 | 51/18723 | 9.90e-04 | 1.18e-02 | 10 |
GO:00300735 | Stomach | GC | insulin secretion | 24/1159 | 195/18723 | 1.01e-03 | 1.20e-02 | 24 |
Page: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0501220 | Cervix | CC | Parkinson disease | 102/1267 | 266/8465 | 1.81e-21 | 1.47e-19 | 8.66e-20 | 102 |
hsa0502018 | Cervix | CC | Prion disease | 98/1267 | 273/8465 | 2.64e-18 | 1.42e-16 | 8.42e-17 | 98 |
hsa0501018 | Cervix | CC | Alzheimer disease | 113/1267 | 384/8465 | 9.67e-14 | 3.92e-12 | 2.32e-12 | 113 |
hsa0502218 | Cervix | CC | Pathways of neurodegeneration - multiple diseases | 128/1267 | 476/8465 | 2.87e-12 | 9.29e-11 | 5.50e-11 | 128 |
hsa0501418 | Cervix | CC | Amyotrophic lateral sclerosis | 103/1267 | 364/8465 | 1.79e-11 | 4.47e-10 | 2.64e-10 | 103 |
hsa0421810 | Cervix | CC | Cellular senescence | 49/1267 | 156/8465 | 1.30e-07 | 1.63e-06 | 9.61e-07 | 49 |
hsa0501716 | Cervix | CC | Spinocerebellar ataxia | 35/1267 | 143/8465 | 1.77e-03 | 7.21e-03 | 4.26e-03 | 35 |
hsa046213 | Cervix | CC | NOD-like receptor signaling pathway | 41/1267 | 186/8465 | 5.90e-03 | 1.95e-02 | 1.15e-02 | 41 |
hsa05012110 | Cervix | CC | Parkinson disease | 102/1267 | 266/8465 | 1.81e-21 | 1.47e-19 | 8.66e-20 | 102 |
hsa0502019 | Cervix | CC | Prion disease | 98/1267 | 273/8465 | 2.64e-18 | 1.42e-16 | 8.42e-17 | 98 |
hsa0501019 | Cervix | CC | Alzheimer disease | 113/1267 | 384/8465 | 9.67e-14 | 3.92e-12 | 2.32e-12 | 113 |
hsa0502219 | Cervix | CC | Pathways of neurodegeneration - multiple diseases | 128/1267 | 476/8465 | 2.87e-12 | 9.29e-11 | 5.50e-11 | 128 |
hsa0501419 | Cervix | CC | Amyotrophic lateral sclerosis | 103/1267 | 364/8465 | 1.79e-11 | 4.47e-10 | 2.64e-10 | 103 |
hsa0421815 | Cervix | CC | Cellular senescence | 49/1267 | 156/8465 | 1.30e-07 | 1.63e-06 | 9.61e-07 | 49 |
hsa0501717 | Cervix | CC | Spinocerebellar ataxia | 35/1267 | 143/8465 | 1.77e-03 | 7.21e-03 | 4.26e-03 | 35 |
hsa0462112 | Cervix | CC | NOD-like receptor signaling pathway | 41/1267 | 186/8465 | 5.90e-03 | 1.95e-02 | 1.15e-02 | 41 |
hsa05012 | Colorectum | AD | Parkinson disease | 147/2092 | 266/8465 | 2.53e-27 | 8.48e-25 | 5.41e-25 | 147 |
hsa05010 | Colorectum | AD | Alzheimer disease | 174/2092 | 384/8465 | 1.82e-19 | 9.26e-18 | 5.91e-18 | 174 |
hsa05020 | Colorectum | AD | Prion disease | 133/2092 | 273/8465 | 2.47e-18 | 8.29e-17 | 5.29e-17 | 133 |
hsa05014 | Colorectum | AD | Amyotrophic lateral sclerosis | 164/2092 | 364/8465 | 4.28e-18 | 1.27e-16 | 8.09e-17 | 164 |
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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 |
MCU | SNV | Missense_Mutation | novel | c.10G>A | p.Ala4Thr | p.A4T | Q8NE86 | protein_coding | tolerated_low_confidence(0.61) | benign(0.001) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
MCU | SNV | Missense_Mutation | novel | c.730N>A | p.Ala244Thr | p.A244T | Q8NE86 | protein_coding | deleterious(0.05) | possibly_damaging(0.771) | TCGA-AA-A01K-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Chemotherapy | folinic | CR |
MCU | SNV | Missense_Mutation | novel | c.494G>T | p.Arg165Ile | p.R165I | Q8NE86 | protein_coding | deleterious(0.04) | benign(0.246) | TCGA-AZ-4315-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
MCU | SNV | Missense_Mutation | rs760003771 | c.721G>A | p.Ala241Thr | p.A241T | Q8NE86 | protein_coding | deleterious(0) | probably_damaging(0.978) | TCGA-CK-5916-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
MCU | SNV | Missense_Mutation | rs770146478 | c.857N>A | p.Arg286His | p.R286H | Q8NE86 | protein_coding | deleterious(0) | possibly_damaging(0.883) | TCGA-AG-A002-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
MCU | insertion | Frame_Shift_Ins | novel | c.952_953insTATGT | p.Asn318IlefsTer19 | p.N318Ifs*19 | Q8NE86 | protein_coding | TCGA-AM-5820-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | ||
MCU | SNV | Missense_Mutation | novel | c.767N>T | p.Trp256Leu | p.W256L | Q8NE86 | protein_coding | deleterious(0) | probably_damaging(0.968) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
MCU | SNV | Missense_Mutation | c.884N>T | p.Arg295Ile | p.R295I | Q8NE86 | protein_coding | deleterious(0) | possibly_damaging(0.756) | TCGA-AP-A0LM-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | cisplatin | SD | |
MCU | SNV | Missense_Mutation | c.376N>A | p.Ala126Thr | p.A126T | Q8NE86 | protein_coding | tolerated(0.13) | benign(0.135) | TCGA-AX-A05S-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | III/IV | Unspecific | Carboplatin & Paclitaxel | PD | |
MCU | SNV | Missense_Mutation | novel | c.424N>T | p.Asp142Tyr | p.D142Y | Q8NE86 | protein_coding | deleterious(0) | benign(0.403) | TCGA-AX-A05Z-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | adriamycin | 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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