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Gene: MRPS35 |
Gene summary for MRPS35 |
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Gene information | Species | Human | Gene symbol | MRPS35 | Gene ID | 60488 |
Gene name | mitochondrial ribosomal protein S35 | |
Gene Alias | HDCMD11P | |
Cytomap | 12p11.22 | |
Gene Type | protein-coding | GO ID | GO:0006412 | UniProtAcc | P82673 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
60488 | MRPS35 | P130T-E | Human | Esophagus | ESCC | 1.90e-78 | 2.09e+00 | 0.1676 |
60488 | MRPS35 | S43 | Human | Liver | Cirrhotic | 8.53e-06 | -2.08e-01 | -0.0187 |
60488 | MRPS35 | HCC1_Meng | Human | Liver | HCC | 1.54e-81 | 2.48e-01 | 0.0246 |
60488 | MRPS35 | HCC2_Meng | Human | Liver | HCC | 6.02e-29 | 7.94e-02 | 0.0107 |
60488 | MRPS35 | cirrhotic1 | Human | Liver | Cirrhotic | 3.67e-02 | 1.62e-02 | 0.0202 |
60488 | MRPS35 | cirrhotic2 | Human | Liver | Cirrhotic | 1.11e-13 | 1.63e-01 | 0.0201 |
60488 | MRPS35 | cirrhotic3 | Human | Liver | Cirrhotic | 2.80e-03 | -4.80e-02 | 0.0215 |
60488 | MRPS35 | HCC1 | Human | Liver | HCC | 1.03e-08 | 3.98e+00 | 0.5336 |
60488 | MRPS35 | HCC2 | Human | Liver | HCC | 2.14e-11 | 3.87e+00 | 0.5341 |
60488 | MRPS35 | Pt13.b | Human | Liver | HCC | 5.97e-17 | 1.26e-01 | 0.0251 |
60488 | MRPS35 | Pt14.a | Human | Liver | HCC | 1.41e-03 | 1.81e-01 | 0.0169 |
60488 | MRPS35 | S014 | Human | Liver | HCC | 5.06e-25 | 1.16e+00 | 0.2254 |
60488 | MRPS35 | S015 | Human | Liver | HCC | 6.56e-20 | 1.26e+00 | 0.2375 |
60488 | MRPS35 | S016 | Human | Liver | HCC | 4.87e-23 | 1.21e+00 | 0.2243 |
60488 | MRPS35 | S027 | Human | Liver | HCC | 1.31e-08 | 1.39e+00 | 0.2446 |
60488 | MRPS35 | S028 | Human | Liver | HCC | 8.98e-22 | 1.44e+00 | 0.2503 |
60488 | MRPS35 | S029 | Human | Liver | HCC | 1.62e-21 | 1.56e+00 | 0.2581 |
60488 | MRPS35 | C04 | Human | Oral cavity | OSCC | 7.19e-32 | 1.62e+00 | 0.2633 |
60488 | MRPS35 | C21 | Human | Oral cavity | OSCC | 1.62e-63 | 2.09e+00 | 0.2678 |
60488 | MRPS35 | C30 | Human | Oral cavity | OSCC | 2.01e-41 | 2.01e+00 | 0.3055 |
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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:0042769 | Colorectum | AD | DNA damage response, detection of DNA damage | 8/3918 | 13/18723 | 1.70e-03 | 1.41e-02 | 8 |
GO:00427691 | Colorectum | MSS | DNA damage response, detection of DNA damage | 7/3467 | 13/18723 | 4.46e-03 | 3.15e-02 | 7 |
GO:00427692 | Colorectum | MSI-H | DNA damage response, detection of DNA damage | 6/1319 | 13/18723 | 1.35e-04 | 3.98e-03 | 6 |
GO:014005313 | Esophagus | ESCC | mitochondrial gene expression | 93/8552 | 108/18723 | 1.96e-18 | 2.03e-16 | 93 |
GO:003254314 | Esophagus | ESCC | mitochondrial translation | 68/8552 | 76/18723 | 1.02e-15 | 6.86e-14 | 68 |
GO:00427697 | Esophagus | ESCC | DNA damage response, detection of DNA damage | 12/8552 | 13/18723 | 6.18e-04 | 3.32e-03 | 12 |
GO:0032543 | Liver | Cirrhotic | mitochondrial translation | 40/4634 | 76/18723 | 1.61e-07 | 4.29e-06 | 40 |
GO:0140053 | Liver | Cirrhotic | mitochondrial gene expression | 49/4634 | 108/18723 | 2.35e-06 | 4.31e-05 | 49 |
GO:00427693 | Liver | Cirrhotic | DNA damage response, detection of DNA damage | 10/4634 | 13/18723 | 1.14e-04 | 1.14e-03 | 10 |
GO:01400531 | Liver | HCC | mitochondrial gene expression | 82/7958 | 108/18723 | 1.49e-12 | 7.20e-11 | 82 |
GO:00325431 | Liver | HCC | mitochondrial translation | 62/7958 | 76/18723 | 2.95e-12 | 1.34e-10 | 62 |
GO:004276911 | Liver | HCC | DNA damage response, detection of DNA damage | 11/7958 | 13/18723 | 2.38e-03 | 1.16e-02 | 11 |
GO:01400533 | Oral cavity | OSCC | mitochondrial gene expression | 78/7305 | 108/18723 | 2.37e-12 | 9.86e-11 | 78 |
GO:00325434 | Oral cavity | OSCC | mitochondrial translation | 59/7305 | 76/18723 | 7.21e-12 | 2.70e-10 | 59 |
GO:00427696 | Oral cavity | OSCC | DNA damage response, detection of DNA damage | 11/7305 | 13/18723 | 1.02e-03 | 5.29e-03 | 11 |
GO:003254313 | Oral cavity | LP | mitochondrial translation | 43/4623 | 76/18723 | 2.85e-09 | 1.26e-07 | 43 |
GO:014005312 | Oral cavity | LP | mitochondrial gene expression | 53/4623 | 108/18723 | 3.54e-08 | 1.27e-06 | 53 |
GO:004276913 | Oral cavity | LP | DNA damage response, detection of DNA damage | 9/4623 | 13/18723 | 8.93e-04 | 7.64e-03 | 9 |
GO:00325436 | Skin | cSCC | mitochondrial translation | 47/4864 | 76/18723 | 4.70e-11 | 2.22e-09 | 47 |
GO:01400535 | Skin | cSCC | mitochondrial gene expression | 56/4864 | 108/18723 | 8.06e-09 | 2.56e-07 | 56 |
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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 |
MRPS35 | SNV | Missense_Mutation | novel | c.298N>A | p.Glu100Lys | p.E100K | P82673 | protein_coding | tolerated(0.36) | benign(0.012) | TCGA-A2-A0YK-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cytoxan | SD |
MRPS35 | SNV | Missense_Mutation | novel | c.86N>A | p.Ala29Asp | p.A29D | P82673 | protein_coding | tolerated_low_confidence(0.38) | benign(0.01) | TCGA-A8-A09K-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
MRPS35 | SNV | Missense_Mutation | c.473C>T | p.Ser158Leu | p.S158L | P82673 | protein_coding | tolerated(0.34) | benign(0.271) | TCGA-AN-A0XW-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD | |
MRPS35 | SNV | Missense_Mutation | c.963T>A | p.Asn321Lys | p.N321K | P82673 | protein_coding | tolerated(0.07) | benign(0.003) | TCGA-AA-A02R-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
MRPS35 | SNV | Missense_Mutation | novel | c.941N>G | p.Glu314Gly | p.E314G | P82673 | protein_coding | deleterious(0) | benign(0.365) | TCGA-AM-5820-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
MRPS35 | SNV | Missense_Mutation | c.383A>T | p.Asp128Val | p.D128V | P82673 | protein_coding | deleterious(0.04) | benign(0.115) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
MRPS35 | insertion | Frame_Shift_Ins | novel | c.942_943insGCTCT | p.Ser315AlafsTer4 | p.S315Afs*4 | P82673 | protein_coding | TCGA-AM-5820-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | ||
MRPS35 | SNV | Missense_Mutation | novel | c.928T>G | p.Ser310Ala | p.S310A | P82673 | protein_coding | tolerated(0.58) | benign(0.001) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
MRPS35 | SNV | Missense_Mutation | rs763066388 | c.421N>A | p.Glu141Lys | p.E141K | P82673 | protein_coding | deleterious(0.03) | probably_damaging(0.962) | TCGA-AJ-A3EL-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
MRPS35 | SNV | Missense_Mutation | novel | c.682N>A | p.Val228Met | p.V228M | P82673 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-AX-A1CE-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unspecific | Paclitaxel | 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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