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Gene: SLC52A2 |
Gene summary for SLC52A2 |
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Gene information | Species | Human | Gene symbol | SLC52A2 | Gene ID | 79581 |
Gene name | solute carrier family 52 member 2 | |
Gene Alias | BVVLS2 | |
Cytomap | 8q24.3 | |
Gene Type | protein-coding | GO ID | GO:0006766 | UniProtAcc | Q9HAB3 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
79581 | SLC52A2 | GSM4909281 | Human | Breast | IDC | 6.45e-21 | 5.74e-01 | 0.21 |
79581 | SLC52A2 | GSM4909285 | Human | Breast | IDC | 4.13e-09 | 3.13e-01 | 0.21 |
79581 | SLC52A2 | GSM4909311 | Human | Breast | IDC | 5.96e-07 | 7.38e-02 | 0.1534 |
79581 | SLC52A2 | GSM4909312 | Human | Breast | IDC | 4.84e-09 | 3.93e-01 | 0.1552 |
79581 | SLC52A2 | GSM4909317 | Human | Breast | IDC | 2.94e-04 | 3.35e-01 | 0.1355 |
79581 | SLC52A2 | GSM4909319 | Human | Breast | IDC | 2.56e-16 | 1.24e-01 | 0.1563 |
79581 | SLC52A2 | GSM4909321 | Human | Breast | IDC | 7.53e-03 | 2.24e-01 | 0.1559 |
79581 | SLC52A2 | brca1 | Human | Breast | Precancer | 6.20e-03 | 2.94e-01 | -0.0338 |
79581 | SLC52A2 | brca2 | Human | Breast | Precancer | 2.85e-06 | 2.65e-01 | -0.024 |
79581 | SLC52A2 | NCCBC5 | Human | Breast | DCIS | 3.16e-03 | 2.77e-02 | 0.2046 |
79581 | SLC52A2 | P1 | Human | Breast | IDC | 1.23e-02 | -1.15e-01 | 0.1527 |
79581 | SLC52A2 | DCIS2 | Human | Breast | DCIS | 1.14e-30 | 8.19e-02 | 0.0085 |
79581 | SLC52A2 | HTA11_2487_2000001011 | Human | Colorectum | SER | 1.24e-02 | 3.26e-01 | -0.1808 |
79581 | SLC52A2 | HTA11_1938_2000001011 | Human | Colorectum | AD | 1.05e-04 | 4.10e-01 | -0.0811 |
79581 | SLC52A2 | HTA11_347_2000001011 | Human | Colorectum | AD | 4.80e-04 | 2.51e-01 | -0.1954 |
79581 | SLC52A2 | HTA11_2112_2000001011 | Human | Colorectum | SER | 6.38e-03 | 5.98e-01 | -0.2196 |
79581 | SLC52A2 | HTA11_696_2000001011 | Human | Colorectum | AD | 6.04e-04 | 2.37e-01 | -0.1464 |
79581 | SLC52A2 | HTA11_866_2000001011 | Human | Colorectum | AD | 8.13e-05 | 2.02e-01 | -0.1001 |
79581 | SLC52A2 | HTA11_1391_2000001011 | Human | Colorectum | AD | 4.57e-09 | 5.41e-01 | -0.059 |
79581 | SLC52A2 | HTA11_7696_3000711011 | Human | Colorectum | AD | 6.70e-07 | 2.91e-01 | 0.0674 |
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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:00467182 | Colorectum | MSS | viral entry into host cell | 47/3467 | 144/18723 | 3.35e-05 | 6.56e-04 | 47 |
GO:00444092 | Colorectum | MSS | entry into host | 47/3467 | 151/18723 | 1.24e-04 | 1.91e-03 | 47 |
GO:0016032111 | Esophagus | ESCC | viral process | 301/8552 | 415/18723 | 3.34e-29 | 1.32e-26 | 301 |
GO:0019058111 | Esophagus | ESCC | viral life cycle | 226/8552 | 317/18723 | 1.17e-20 | 1.76e-18 | 226 |
GO:0044403111 | Esophagus | ESCC | biological process involved in symbiotic interaction | 186/8552 | 290/18723 | 1.43e-10 | 4.16e-09 | 186 |
GO:0051701111 | Esophagus | ESCC | biological process involved in interaction with host | 135/8552 | 203/18723 | 1.49e-09 | 3.49e-08 | 135 |
GO:0052126111 | Esophagus | ESCC | movement in host environment | 117/8552 | 175/18723 | 1.14e-08 | 2.26e-07 | 117 |
GO:0044409111 | Esophagus | ESCC | entry into host | 96/8552 | 151/18723 | 6.73e-06 | 6.84e-05 | 96 |
GO:004671827 | Esophagus | ESCC | viral entry into host cell | 89/8552 | 144/18723 | 6.84e-05 | 5.18e-04 | 89 |
GO:00067671 | Esophagus | ESCC | water-soluble vitamin metabolic process | 41/8552 | 59/18723 | 1.84e-04 | 1.17e-03 | 41 |
GO:00067661 | Esophagus | ESCC | vitamin metabolic process | 67/8552 | 106/18723 | 2.03e-04 | 1.28e-03 | 67 |
GO:001603222 | Liver | HCC | viral process | 286/7958 | 415/18723 | 4.41e-28 | 1.86e-25 | 286 |
GO:001905822 | Liver | HCC | viral life cycle | 209/7958 | 317/18723 | 2.05e-17 | 2.09e-15 | 209 |
GO:004440322 | Liver | HCC | biological process involved in symbiotic interaction | 183/7958 | 290/18723 | 9.13e-13 | 4.59e-11 | 183 |
GO:005170122 | Liver | HCC | biological process involved in interaction with host | 128/7958 | 203/18723 | 2.51e-09 | 6.91e-08 | 128 |
GO:005212612 | Liver | HCC | movement in host environment | 109/7958 | 175/18723 | 9.58e-08 | 1.89e-06 | 109 |
GO:004440912 | Liver | HCC | entry into host | 88/7958 | 151/18723 | 6.47e-05 | 5.91e-04 | 88 |
GO:004671812 | Liver | HCC | viral entry into host cell | 83/7958 | 144/18723 | 1.73e-04 | 1.36e-03 | 83 |
GO:0006767 | Liver | HCC | water-soluble vitamin metabolic process | 39/7958 | 59/18723 | 2.14e-04 | 1.63e-03 | 39 |
GO:0006766 | Liver | HCC | vitamin metabolic process | 57/7958 | 106/18723 | 1.25e-02 | 4.53e-02 | 57 |
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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 |
SLC52A2 | SNV | Missense_Mutation | c.342N>G | p.Phe114Leu | p.F114L | Q9HAB3 | protein_coding | tolerated(0.31) | benign(0.003) | TCGA-C8-A274-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | tamoxiphen | SD | |
SLC52A2 | SNV | Missense_Mutation | rs781873022 | c.1289A>G | p.Tyr430Cys | p.Y430C | Q9HAB3 | protein_coding | deleterious(0.01) | benign(0.253) | TCGA-E2-A1B4-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Hormone Therapy | arimidex | SD |
SLC52A2 | insertion | Frame_Shift_Ins | novel | c.381_382insCAAGACTCCTGGGCTGCGG | p.Ser128GlnfsTer68 | p.S128Qfs*68 | Q9HAB3 | protein_coding | TCGA-A2-A0D1-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | taxotere | SD | ||
SLC52A2 | deletion | Frame_Shift_Del | c.979delC | p.Leu327TrpfsTer27 | p.L327Wfs*27 | Q9HAB3 | protein_coding | TCGA-BH-A0C1-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | adriamycin | PD | |||
SLC52A2 | deletion | Frame_Shift_Del | novel | c.884delC | p.Pro295LeufsTer59 | p.P295Lfs*59 | Q9HAB3 | protein_coding | TCGA-EW-A2FV-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | docetaxel | SD | ||
SLC52A2 | SNV | Missense_Mutation | rs782253510 | c.1019N>A | p.Gly340Asp | p.G340D | Q9HAB3 | protein_coding | deleterious(0.01) | possibly_damaging(0.653) | TCGA-DS-A0VM-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | PD |
SLC52A2 | SNV | Missense_Mutation | c.1028N>T | p.Ser343Phe | p.S343F | Q9HAB3 | protein_coding | deleterious(0.03) | benign(0.033) | TCGA-3L-AA1B-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
SLC52A2 | SNV | Missense_Mutation | c.307N>A | p.Ala103Thr | p.A103T | Q9HAB3 | protein_coding | tolerated(0.48) | benign(0.001) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
SLC52A2 | SNV | Missense_Mutation | rs144883729 | c.613N>A | p.Val205Ile | p.V205I | Q9HAB3 | protein_coding | tolerated(0.15) | benign(0.073) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
SLC52A2 | SNV | Missense_Mutation | c.736N>A | p.Glu246Lys | p.E246K | Q9HAB3 | protein_coding | tolerated(0.2) | benign(0.081) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
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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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