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Gene: MR1 |
Gene summary for MR1 |
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Gene information | Species | Human | Gene symbol | MR1 | Gene ID | 3140 |
Gene name | major histocompatibility complex, class I-related | |
Gene Alias | HLALS | |
Cytomap | 1q25.3 | |
Gene Type | protein-coding | GO ID | GO:0001775 | UniProtAcc | Q95460 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
3140 | MR1 | C51 | Human | Oral cavity | OSCC | 6.83e-06 | 4.13e-01 | 0.2674 |
3140 | MR1 | C08 | Human | Oral cavity | OSCC | 1.14e-11 | 3.27e-01 | 0.1919 |
3140 | MR1 | SYSMH1 | Human | Oral cavity | OSCC | 6.11e-04 | 1.83e-01 | 0.1127 |
3140 | MR1 | SYSMH2 | Human | Oral cavity | OSCC | 2.16e-03 | 2.04e-01 | 0.2326 |
3140 | MR1 | 052095_1628-all-cells | Human | Prostate | BPH | 1.42e-03 | 1.40e-01 | 0.1032 |
3140 | MR1 | Dong_P3 | Human | Prostate | Tumor | 1.86e-06 | 1.68e-01 | 0.0278 |
3140 | MR1 | GSM5353221_PA_PB2A_Pool_1_3_S25_L001 | Human | Prostate | Tumor | 9.22e-08 | 5.34e-01 | 0.1633 |
3140 | MR1 | GSM5353222_PA_PB2B_Pool_1_3_S52_L002 | Human | Prostate | Tumor | 5.37e-03 | 3.09e-01 | 0.1608 |
3140 | MR1 | GSM5353223_PA_PB2B_Pool_2_S26_L001 | Human | Prostate | Tumor | 2.47e-05 | 4.68e-01 | 0.1604 |
3140 | MR1 | GSM5353227_PA_PR5199-193K_Pool_1_2_3_S55_L002 | Human | Prostate | Tumor | 5.45e-03 | 3.92e-01 | 0.1602 |
3140 | MR1 | GSM5353237_PA_PR5251_T2_S8_L001 | Human | Prostate | Tumor | 2.40e-02 | 5.43e-01 | 0.1622 |
3140 | MR1 | GSM5353248_PA_PR5269_4_S28_L002 | Human | Prostate | Tumor | 2.46e-03 | 7.23e-01 | 0.1541 |
3140 | MR1 | male-WTA | Human | Thyroid | PTC | 1.73e-10 | 1.51e-01 | 0.1037 |
3140 | MR1 | PTC01 | Human | Thyroid | PTC | 2.99e-07 | 1.13e-01 | 0.1899 |
3140 | MR1 | PTC04 | Human | Thyroid | PTC | 1.71e-07 | 1.77e-01 | 0.1927 |
3140 | MR1 | PTC05 | Human | Thyroid | PTC | 7.18e-19 | 5.59e-01 | 0.2065 |
3140 | MR1 | PTC06 | Human | Thyroid | PTC | 3.56e-24 | 5.19e-01 | 0.2057 |
3140 | MR1 | PTC07 | Human | Thyroid | PTC | 3.19e-19 | 3.56e-01 | 0.2044 |
3140 | MR1 | ATC13 | Human | Thyroid | ATC | 1.43e-06 | 7.49e-02 | 0.34 |
3140 | MR1 | ATC2 | Human | Thyroid | ATC | 3.72e-02 | 1.87e-01 | 0.34 |
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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:0016311 | Colorectum | AD | dephosphorylation | 123/3918 | 417/18723 | 1.84e-05 | 3.82e-04 | 123 |
GO:0030258 | Colorectum | AD | lipid modification | 67/3918 | 212/18723 | 1.66e-04 | 2.27e-03 | 67 |
GO:0006650 | Colorectum | AD | glycerophospholipid metabolic process | 83/3918 | 306/18723 | 5.40e-03 | 3.55e-02 | 83 |
GO:0006644 | Colorectum | AD | phospholipid metabolic process | 101/3918 | 383/18723 | 5.80e-03 | 3.67e-02 | 101 |
GO:0046486 | Colorectum | SER | glycerolipid metabolic process | 82/2897 | 392/18723 | 2.26e-03 | 2.17e-02 | 82 |
GO:00163111 | Colorectum | SER | dephosphorylation | 86/2897 | 417/18723 | 2.73e-03 | 2.46e-02 | 86 |
GO:00066441 | Colorectum | SER | phospholipid metabolic process | 79/2897 | 383/18723 | 3.94e-03 | 3.24e-02 | 79 |
GO:00302581 | Colorectum | SER | lipid modification | 47/2897 | 212/18723 | 6.01e-03 | 4.38e-02 | 47 |
GO:00066501 | Colorectum | SER | glycerophospholipid metabolic process | 64/2897 | 306/18723 | 6.41e-03 | 4.60e-02 | 64 |
GO:00302582 | Colorectum | MSS | lipid modification | 57/3467 | 212/18723 | 1.64e-03 | 1.49e-02 | 57 |
GO:00163112 | Colorectum | MSS | dephosphorylation | 101/3467 | 417/18723 | 1.98e-03 | 1.70e-02 | 101 |
GO:00163113 | Colorectum | FAP | dephosphorylation | 95/2622 | 417/18723 | 7.07e-07 | 3.32e-05 | 95 |
GO:00302583 | Colorectum | FAP | lipid modification | 52/2622 | 212/18723 | 2.84e-05 | 6.49e-04 | 52 |
GO:00066502 | Colorectum | FAP | glycerophospholipid metabolic process | 62/2622 | 306/18723 | 1.54e-03 | 1.38e-02 | 62 |
GO:00066442 | Colorectum | FAP | phospholipid metabolic process | 74/2622 | 383/18723 | 2.24e-03 | 1.83e-02 | 74 |
GO:19019984 | Endometrium | EEC | toxin transport | 11/2168 | 40/18723 | 4.65e-03 | 2.97e-02 | 11 |
GO:0008380111 | Esophagus | ESCC | RNA splicing | 336/8552 | 434/18723 | 1.74e-42 | 3.67e-39 | 336 |
GO:0010498111 | Esophagus | ESCC | proteasomal protein catabolic process | 369/8552 | 490/18723 | 1.13e-41 | 1.80e-38 | 369 |
GO:0002181111 | Esophagus | ESCC | cytoplasmic translation | 135/8552 | 148/18723 | 4.17e-32 | 2.65e-29 | 135 |
GO:0000375111 | Esophagus | ESCC | RNA splicing, via transesterification reactions | 248/8552 | 324/18723 | 3.05e-30 | 1.49e-27 | 248 |
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 28 29 30 31 32 33 34 35 36 37 38 |
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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 |
MR1 | SNV | Missense_Mutation | c.1022G>A | p.Arg341Gln | p.R341Q | Q95460 | protein_coding | tolerated_low_confidence(1) | benign(0) | TCGA-A8-A095-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | 5-fluorouracil | CR | |
MR1 | SNV | Missense_Mutation | c.334C>G | p.His112Asp | p.H112D | Q95460 | protein_coding | deleterious(0) | benign(0.393) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
MR1 | SNV | Missense_Mutation | c.176A>G | p.Asp59Gly | p.D59G | Q95460 | protein_coding | deleterious(0) | benign(0.371) | TCGA-BH-A18G-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
MR1 | SNV | Missense_Mutation | c.65N>T | p.Ser22Phe | p.S22F | Q95460 | protein_coding | deleterious(0.01) | benign(0.06) | TCGA-D8-A1JA-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | adriamycin | PD | |
MR1 | SNV | Missense_Mutation | novel | c.382A>G | p.Thr128Ala | p.T128A | Q95460 | protein_coding | tolerated(0.08) | possibly_damaging(0.682) | TCGA-OL-A6VR-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
MR1 | SNV | Missense_Mutation | novel | c.148G>A | p.Val50Met | p.V50M | Q95460 | protein_coding | deleterious(0.01) | probably_damaging(0.999) | TCGA-DS-A1OB-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | carboplatin | PD |
MR1 | SNV | Missense_Mutation | novel | c.823N>G | p.Leu275Val | p.L275V | Q95460 | protein_coding | tolerated(0.62) | benign(0.005) | TCGA-VS-A8EK-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Chemotherapy | cisplatin | PD |
MR1 | SNV | Missense_Mutation | rs377066166 | c.816N>A | p.Ser272Arg | p.S272R | Q95460 | protein_coding | deleterious(0.04) | possibly_damaging(0.452) | TCGA-A6-6782-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
MR1 | SNV | Missense_Mutation | rs775161220 | c.137C>T | p.Ser46Leu | p.S46L | Q95460 | protein_coding | tolerated(0.1) | probably_damaging(0.998) | TCGA-AA-3510-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
MR1 | SNV | Missense_Mutation | rs775161220 | c.137C>T | p.Ser46Leu | p.S46L | Q95460 | protein_coding | tolerated(0.1) | probably_damaging(0.998) | TCGA-AA-3977-01 | 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 |
3140 | MR1 | DRUGGABLE GENOME, EXTERNAL SIDE OF PLASMA MEMBRANE | ANTITHYMOCYTE GLOBULIN |
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